Canonical Allele Identifier: CA32777194
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs370533988
gnomAD v2: 1-173872998-T-C
gnomAD v3: 1-173903860-T-C
gnomAD v4: 1-173903860-T-C
MyVariant Identifiers: chr1:g.173872998T>C (hg19) chr1:g.173903860T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903860T>C , CM000663.2:g.173903860T>C GRCh38
NC_000001.10:g.173872998T>C , CM000663.1:g.173872998T>C GRCh37
NC_000001.9:g.172139621T>C NCBI36
NG_012462.1:g.18519A>G , LRG_577:g.18519A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.*29A>G MANE Select ENSP00000356671.3:n.*29A>G
ENST00000367698.3:c.*29A>G ENSP00000356671.3:n.*29A>G
ENST00000617423.4:c.*29A>G ENSP00000478688.1:n.*29A>G
NM_000488.3:c.*29A>G , LRG_577t1:c.*29A>G NP_000479.1:n.*29A>G
XM_005245198.2:c.*29A>G XP_005245255.1:n.*29A>G
NM_001365052.1:c.*29A>G NP_001351981.1:n.*29A>G
NM_000488.4:c.*29A>G MANE Select NP_000479.1:n.*29A>G
NM_001365052.2:c.*29A>G NP_001351981.1:n.*29A>G
NM_001386302.1:c.*29A>G NP_001373231.1:n.*29A>G
NM_001386303.1:c.*29A>G NP_001373232.1:n.*29A>G
NM_001386304.1:c.*29A>G NP_001373233.1:n.*29A>G
NM_001386305.1:c.*29A>G NP_001373234.1:n.*29A>G
NM_001386306.1:c.*29A>G NP_001373235.1:n.*29A>G
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