Canonical Allele Identifier: CA1266820001
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545964C= , CM000664.2:g.85545964C= GRCh38
NC_000002.11:g.85773087C= , CM000664.1:g.85773087C= GRCh37
NC_000002.10:g.85626598C= NCBI36
NG_011811.2:g.20571G=
NG_029183.1:g.11987C=

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3970G= MANE Select ENSP00000233838.3:n.*3970G=
ENST00000233838.8:c.*3970G= ENSP00000233838.3:n.*3970G=
NM_000821.5:c.*3970G= NP_000812.2:n.*3970G=
NM_000821.6:c.*3970G= NP_000812.2:n.*3970G=
NM_001142269.2:c.*3970G= NP_001135741.1:n.*3970G=
NM_001142269.3:c.*3970G= NP_001135741.1:n.*3970G=
NM_000821.7:c.*3970G= MANE Select NP_000812.2:n.*3970G=
NM_001142269.4:c.*3970G= NP_001135741.1:n.*3970G=