Canonical Allele Identifier: CA1251210
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs753725301

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903877A>C , CM000663.2:g.173903877A>C GRCh38
NC_000001.10:g.173873015A>C , CM000663.1:g.173873015A>C GRCh37
NC_000001.9:g.172139638A>C NCBI36
NG_012462.1:g.18502T>G , LRG_577:g.18502T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.*12T>G MANE Select ENSP00000356671.3:n.*12T>G
ENST00000367698.3:c.*12T>G ENSP00000356671.3:n.*12T>G
ENST00000617423.4:c.*12T>G ENSP00000478688.1:n.*12T>G
NM_000488.3:c.*12T>G , LRG_577t1:c.*12T>G NP_000479.1:n.*12T>G
XM_005245198.2:c.*12T>G XP_005245255.1:n.*12T>G
NM_001365052.1:c.*12T>G NP_001351981.1:n.*12T>G
NM_000488.4:c.*12T>G MANE Select NP_000479.1:n.*12T>G
NM_001365052.2:c.*12T>G NP_001351981.1:n.*12T>G
NM_001386302.1:c.*12T>G NP_001373231.1:n.*12T>G
NM_001386303.1:c.*12T>G NP_001373232.1:n.*12T>G
NM_001386304.1:c.*12T>G NP_001373233.1:n.*12T>G
NM_001386305.1:c.*12T>G NP_001373234.1:n.*12T>G
NM_001386306.1:c.*12T>G NP_001373235.1:n.*12T>G