Canonical Allele Identifier: CA343774652
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657695186
gnomAD v3: 1-173909881-T-C
gnomAD v4: 1-173909881-T-C
MyVariant Identifiers: chr1:g.173879019T>C (hg19) chr1:g.173909881T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909881T>C , CM000663.2:g.173909881T>C GRCh38
NC_000001.10:g.173879019T>C , CM000663.1:g.173879019T>C GRCh37
NC_000001.9:g.172145642T>C NCBI36
NG_012462.1:g.12498A>G , LRG_577:g.12498A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.824A>G MANE Select ENSP00000356671.3:p.Asp275Gly
ENST00000367698.3:c.824A>G ENSP00000356671.3:p.Asp275Gly
ENST00000487183.1:n.475A>G
ENST00000617423.4:c.559+1983A>G ENSP00000478688.1:n.559+1983A>G
NM_000488.3:c.824A>G , LRG_577t1:c.824A>G NP_000479.1:p.Asp275Gly
XM_005245198.2:c.680A>G XP_005245255.1:p.Asp227Gly
NM_001365052.1:c.680A>G NP_001351981.1:p.Asp227Gly
NM_000488.4:c.824A>G MANE Select NP_000479.1:p.Asp275Gly
NM_001365052.2:c.680A>G NP_001351981.1:p.Asp227Gly
NM_001386302.1:c.947A>G NP_001373231.1:p.Asp316Gly
NM_001386303.1:c.905A>G NP_001373232.1:p.Asp302Gly
NM_001386304.1:c.803A>G NP_001373233.1:p.Asp268Gly
NM_001386305.1:c.767A>G NP_001373234.1:p.Asp256Gly
NM_001386306.1:c.608A>G NP_001373235.1:p.Asp203Gly
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