Canonical Allele Identifier: CA1266820864
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546466C= , CM000664.2:g.85546466C= GRCh38
NC_000002.11:g.85773589C= , CM000664.1:g.85773589C= GRCh37
NC_000002.10:g.85627100C= NCBI36
NG_011811.2:g.20069G=
NG_029183.1:g.12489C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3468G= MANE Select ENSP00000233838.3:n.*3468G=
ENST00000233838.8:c.*3468G= ENSP00000233838.3:n.*3468G=
NM_000821.5:c.*3468G= NP_000812.2:n.*3468G=
NM_000821.6:c.*3468G= NP_000812.2:n.*3468G=
NM_001142269.2:c.*3468G= NP_001135741.1:n.*3468G=
NM_001142269.3:c.*3468G= NP_001135741.1:n.*3468G=
NM_000821.7:c.*3468G= MANE Select NP_000812.2:n.*3468G=
NM_001142269.4:c.*3468G= NP_001135741.1:n.*3468G=