Canonical Allele Identifier: CA343774368
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878951C>T (hg19) chr1:g.173909813C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909813C>T , CM000663.2:g.173909813C>T GRCh38
NC_000001.10:g.173878951C>T , CM000663.1:g.173878951C>T GRCh37
NC_000001.9:g.172145574C>T NCBI36
NG_012462.1:g.12566G>A , LRG_577:g.12566G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.892G>A MANE Select ENSP00000356671.3:p.Gly298Ser
ENST00000367698.3:c.892G>A ENSP00000356671.3:p.Gly298Ser
ENST00000487183.1:n.543G>A
ENST00000617423.4:c.559+2051G>A ENSP00000478688.1:n.559+2051G>A
NM_000488.3:c.892G>A , LRG_577t1:c.892G>A NP_000479.1:p.Gly298Ser
XM_005245198.2:c.748G>A XP_005245255.1:p.Gly250Ser
NM_001365052.1:c.748G>A NP_001351981.1:p.Gly250Ser
NM_000488.4:c.892G>A MANE Select NP_000479.1:p.Gly298Ser
NM_001365052.2:c.748G>A NP_001351981.1:p.Gly250Ser
NM_001386302.1:c.1015G>A NP_001373231.1:p.Gly339Ser
NM_001386303.1:c.973G>A NP_001373232.1:p.Gly325Ser
NM_001386304.1:c.871G>A NP_001373233.1:p.Gly291Ser
NM_001386305.1:c.835G>A NP_001373234.1:p.Gly279Ser
NM_001386306.1:c.676G>A NP_001373235.1:p.Gly226Ser
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