Canonical Allele Identifier: CA1266820792
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546420A= , CM000664.2:g.85546420A= GRCh38
NC_000002.11:g.85773543A= , CM000664.1:g.85773543A= GRCh37
NC_000002.10:g.85627054A= NCBI36
NG_011811.2:g.20115T=
NG_029183.1:g.12443A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3514T= MANE Select ENSP00000233838.3:n.*3514T=
ENST00000233838.8:c.*3514T= ENSP00000233838.3:n.*3514T=
NM_000821.5:c.*3514T= NP_000812.2:n.*3514T=
NM_000821.6:c.*3514T= NP_000812.2:n.*3514T=
NM_001142269.2:c.*3514T= NP_001135741.1:n.*3514T=
NM_001142269.3:c.*3514T= NP_001135741.1:n.*3514T=
NM_000821.7:c.*3514T= MANE Select NP_000812.2:n.*3514T=
NM_001142269.4:c.*3514T= NP_001135741.1:n.*3514T=