Canonical Allele Identifier: CA1266820923
Gene: GGCX HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546492G= , CM000664.2:g.85546492G= GRCh38
NC_000002.11:g.85773615G= , CM000664.1:g.85773615G= GRCh37
NC_000002.10:g.85627126G= NCBI36
NG_011811.2:g.20043C=
NG_029183.1:g.12515G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3442C= MANE Select ENSP00000233838.3:n.*3442C=
ENST00000233838.8:c.*3442C= ENSP00000233838.3:n.*3442C=
NM_000821.5:c.*3442C= NP_000812.2:n.*3442C=
NM_000821.6:c.*3442C= NP_000812.2:n.*3442C=
NM_001142269.2:c.*3442C= NP_001135741.1:n.*3442C=
NM_001142269.3:c.*3442C= NP_001135741.1:n.*3442C=
NM_000821.7:c.*3442C= MANE Select NP_000812.2:n.*3442C=
NM_001142269.4:c.*3442C= NP_001135741.1:n.*3442C=
Search 100 bp 5'
Search 100 bp 3'