Canonical Allele Identifier: CA343773827
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs755808418
gnomAD v4: 1-173909683-T-A
MyVariant Identifiers: chr1:g.173878821T>A (hg19) chr1:g.173909683T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909683T>A , CM000663.2:g.173909683T>A GRCh38
NC_000001.10:g.173878821T>A , CM000663.1:g.173878821T>A GRCh37
NC_000001.9:g.172145444T>A NCBI36
NG_012462.1:g.12696A>T , LRG_577:g.12696A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1022A>T MANE Select ENSP00000356671.3:p.Asp341Val
ENST00000367698.3:c.1022A>T ENSP00000356671.3:p.Asp341Val
ENST00000617423.4:c.559+2181A>T ENSP00000478688.1:n.559+2181A>T
NM_000488.3:c.1022A>T , LRG_577t1:c.1022A>T NP_000479.1:p.Asp341Val
XM_005245198.2:c.878A>T XP_005245255.1:p.Asp293Val
NM_001365052.1:c.878A>T NP_001351981.1:p.Asp293Val
NM_000488.4:c.1022A>T MANE Select NP_000479.1:p.Asp341Val
NM_001365052.2:c.878A>T NP_001351981.1:p.Asp293Val
NM_001386302.1:c.1145A>T NP_001373231.1:p.Asp382Val
NM_001386303.1:c.1103A>T NP_001373232.1:p.Asp368Val
NM_001386304.1:c.1001A>T NP_001373233.1:p.Asp334Val
NM_001386305.1:c.965A>T NP_001373234.1:p.Asp322Val
NM_001386306.1:c.806A>T NP_001373235.1:p.Asp269Val
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