Canonical Allele Identifier: CA2565358884
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545885T>A , CM000664.2:g.85545885T>A GRCh38
NC_000002.11:g.85773008T>A , CM000664.1:g.85773008T>A GRCh37
NC_000002.10:g.85626519T>A NCBI36
NG_011811.2:g.20650A>T
NG_029183.1:g.11908T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*4049A>T MANE Select ENSP00000233838.3:n.*4049A>T
ENST00000233838.8:c.*4049A>T ENSP00000233838.3:n.*4049A>T
NM_000821.5:c.*4049A>T NP_000812.2:n.*4049A>T
NM_000821.6:c.*4049A>T NP_000812.2:n.*4049A>T
NM_001142269.2:c.*4049A>T NP_001135741.1:n.*4049A>T
NM_001142269.3:c.*4049A>T NP_001135741.1:n.*4049A>T
NM_000821.7:c.*4049A>T MANE Select NP_000812.2:n.*4049A>T
NM_001142269.4:c.*4049A>T NP_001135741.1:n.*4049A>T