Canonical Allele Identifier: CA1266820821
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546432G= , CM000664.2:g.85546432G= GRCh38
NC_000002.11:g.85773555G= , CM000664.1:g.85773555G= GRCh37
NC_000002.10:g.85627066G= NCBI36
NG_011811.2:g.20103C=
NG_029183.1:g.12455G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3502C= MANE Select ENSP00000233838.3:n.*3502C=
ENST00000233838.8:c.*3502C= ENSP00000233838.3:n.*3502C=
NM_000821.5:c.*3502C= NP_000812.2:n.*3502C=
NM_000821.6:c.*3502C= NP_000812.2:n.*3502C=
NM_001142269.2:c.*3502C= NP_001135741.1:n.*3502C=
NM_001142269.3:c.*3502C= NP_001135741.1:n.*3502C=
NM_000821.7:c.*3502C= MANE Select NP_000812.2:n.*3502C=
NM_001142269.4:c.*3502C= NP_001135741.1:n.*3502C=