Canonical Allele Identifier: CA1266819891
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545862T= , CM000664.2:g.85545862T= GRCh38
NC_000002.11:g.85772985T= , CM000664.1:g.85772985T= GRCh37
NC_000002.10:g.85626496T= NCBI36
NG_011811.2:g.20673A=
NG_029183.1:g.11885T=

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4072A= MANE Select ENSP00000233838.3:n.*4072A=
ENST00000233838.8:c.*4072A= ENSP00000233838.3:n.*4072A=
NM_000821.5:c.*4072A= NP_000812.2:n.*4072A=
NM_000821.6:c.*4072A= NP_000812.2:n.*4072A=
NM_001142269.2:c.*4072A= NP_001135741.1:n.*4072A=
NM_001142269.3:c.*4072A= NP_001135741.1:n.*4072A=
NM_000821.7:c.*4072A= MANE Select NP_000812.2:n.*4072A=
NM_001142269.4:c.*4072A= NP_001135741.1:n.*4072A=