Canonical Allele Identifier: CA343774644
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879017C>T (hg19) chr1:g.173909879C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909879C>T , CM000663.2:g.173909879C>T GRCh38
NC_000001.10:g.173879017C>T , CM000663.1:g.173879017C>T GRCh37
NC_000001.9:g.172145640C>T NCBI36
NG_012462.1:g.12500G>A , LRG_577:g.12500G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.826G>A MANE Select ENSP00000356671.3:p.Gly276Arg
ENST00000367698.3:c.826G>A ENSP00000356671.3:p.Gly276Arg
ENST00000487183.1:n.477G>A
ENST00000617423.4:c.559+1985G>A ENSP00000478688.1:n.559+1985G>A
NM_000488.3:c.826G>A , LRG_577t1:c.826G>A NP_000479.1:p.Gly276Arg
XM_005245198.2:c.682G>A XP_005245255.1:p.Gly228Arg
NM_001365052.1:c.682G>A NP_001351981.1:p.Gly228Arg
NM_000488.4:c.826G>A MANE Select NP_000479.1:p.Gly276Arg
NM_001365052.2:c.682G>A NP_001351981.1:p.Gly228Arg
NM_001386302.1:c.949G>A NP_001373231.1:p.Gly317Arg
NM_001386303.1:c.907G>A NP_001373232.1:p.Gly303Arg
NM_001386304.1:c.805G>A NP_001373233.1:p.Gly269Arg
NM_001386305.1:c.769G>A NP_001373234.1:p.Gly257Arg
NM_001386306.1:c.610G>A NP_001373235.1:p.Gly204Arg
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