Canonical Allele Identifier: CA32782455
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs2227598

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173915033G>A , CM000663.2:g.173915033G>A GRCh38
NC_000001.10:g.173884171G>A , CM000663.1:g.173884171G>A GRCh37
NC_000001.9:g.172150794G>A NCBI36
NG_012462.1:g.7346C>T , LRG_577:g.7346C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.42-114C>T MANE Select ENSP00000356671.3:n.42-114C>T
ENST00000367698.3:c.42-114C>T ENSP00000356671.3:n.42-114C>T
ENST00000494024.1:n.252C>T
ENST00000617423.4:c.42-114C>T ENSP00000478688.1:n.42-114C>T
NM_000488.3:c.42-114C>T , LRG_577t1:c.42-114C>T NP_000479.1:n.42-114C>T
XM_005245198.2:c.-119C>T XP_005245255.1:n.-119C>T
NM_001365052.1:c.-119C>T NP_001351981.1:n.-119C>T
NM_000488.4:c.42-114C>T MANE Select NP_000479.1:n.42-114C>T
NM_001365052.2:c.-119C>T NP_001351981.1:n.-119C>T
NM_001386302.1:c.42-114C>T NP_001373231.1:n.42-114C>T
NM_001386303.1:c.123-114C>T NP_001373232.1:n.123-114C>T
NM_001386304.1:c.42-114C>T NP_001373233.1:n.42-114C>T
NM_001386305.1:c.42-114C>T NP_001373234.1:n.42-114C>T
NM_001386306.1:c.42-114C>T NP_001373235.1:n.42-114C>T