Canonical Allele Identifier: CA527601273
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1254205302
gnomAD v2: 1-173879133-T-G
gnomAD v3: 1-173909995-T-G
gnomAD v4: 1-173909995-T-G
MyVariant Identifiers: chr1:g.173879133T>G (hg19) chr1:g.173909995T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909995T>G , CM000663.2:g.173909995T>G GRCh38
NC_000001.10:g.173879133T>G , CM000663.1:g.173879133T>G GRCh37
NC_000001.9:g.172145756T>G NCBI36
NG_012462.1:g.12384A>C , LRG_577:g.12384A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-53A>C MANE Select ENSP00000356671.3:n.763-53A>C
ENST00000367698.3:c.763-53A>C ENSP00000356671.3:n.763-53A>C
ENST00000487183.1:n.414-53A>C
ENST00000617423.4:c.559+1869A>C ENSP00000478688.1:n.559+1869A>C
NM_000488.3:c.763-53A>C , LRG_577t1:c.763-53A>C NP_000479.1:n.763-53A>C
XM_005245198.2:c.619-53A>C XP_005245255.1:n.619-53A>C
NM_001365052.1:c.619-53A>C NP_001351981.1:n.619-53A>C
NM_000488.4:c.763-53A>C MANE Select NP_000479.1:n.763-53A>C
NM_001365052.2:c.619-53A>C NP_001351981.1:n.619-53A>C
NM_001386302.1:c.886-53A>C NP_001373231.1:n.886-53A>C
NM_001386303.1:c.844-53A>C NP_001373232.1:n.844-53A>C
NM_001386304.1:c.742-53A>C NP_001373233.1:n.742-53A>C
NM_001386305.1:c.763-110A>C NP_001373234.1:n.763-110A>C
NM_001386306.1:c.547-53A>C NP_001373235.1:n.547-53A>C
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