Canonical Allele Identifier: CA421943043
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1572091917
MyVariant Identifiers: chr1:g.173883835G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914697G>C , CM000663.2:g.173914697G>C GRCh38
NC_000001.10:g.173883835G>C , CM000663.1:g.173883835G>C GRCh37
NC_000001.9:g.172150458G>C NCBI36
NG_012462.1:g.7682C>G , LRG_577:g.7682C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.264C>G MANE Select ENSP00000356671.3:p.Ser88=
ENST00000367698.3:c.264C>G ENSP00000356671.3:p.Ser88=
ENST00000494024.1:n.490C>G
ENST00000617423.4:c.264C>G ENSP00000478688.1:p.Ser88=
NM_000488.3:c.264C>G , LRG_577t1:c.264C>G NP_000479.1:p.Ser88=
XM_005245198.2:c.120C>G XP_005245255.1:p.Ser40=
NM_001365052.1:c.120C>G NP_001351981.1:p.Ser40=
NM_000488.4:c.264C>G MANE Select NP_000479.1:p.Ser88=
NM_001365052.2:c.120C>G NP_001351981.1:p.Ser40=
NM_001386302.1:c.264C>G NP_001373231.1:p.Ser88=
NM_001386303.1:c.345C>G NP_001373232.1:p.Ser115=
NM_001386304.1:c.264C>G NP_001373233.1:p.Ser88=
NM_001386305.1:c.264C>G NP_001373234.1:p.Ser88=
NM_001386306.1:c.264C>G NP_001373235.1:p.Ser88=