Canonical Allele Identifier: CA894034770
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1443995060

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546390T>A , CM000664.2:g.85546390T>A GRCh38
NC_000002.11:g.85773513T>A , CM000664.1:g.85773513T>A GRCh37
NC_000002.10:g.85627024T>A NCBI36
NG_011811.2:g.20145A>T
NG_029183.1:g.12413T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3544A>T MANE Select ENSP00000233838.3:n.*3544A>T
ENST00000233838.8:c.*3544A>T ENSP00000233838.3:n.*3544A>T
NM_000821.5:c.*3544A>T NP_000812.2:n.*3544A>T
NM_000821.6:c.*3544A>T NP_000812.2:n.*3544A>T
NM_001142269.2:c.*3544A>T NP_001135741.1:n.*3544A>T
NM_001142269.3:c.*3544A>T NP_001135741.1:n.*3544A>T
NM_000821.7:c.*3544A>T MANE Select NP_000812.2:n.*3544A>T
NM_001142269.4:c.*3544A>T NP_001135741.1:n.*3544A>T