Canonical Allele Identifier: CA1266820696
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546395C= , CM000664.2:g.85546395C= GRCh38
NC_000002.11:g.85773518C= , CM000664.1:g.85773518C= GRCh37
NC_000002.10:g.85627029C= NCBI36
NG_011811.2:g.20140G=
NG_029183.1:g.12418C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3539G= MANE Select ENSP00000233838.3:n.*3539G=
ENST00000233838.8:c.*3539G= ENSP00000233838.3:n.*3539G=
NM_000821.5:c.*3539G= NP_000812.2:n.*3539G=
NM_000821.6:c.*3539G= NP_000812.2:n.*3539G=
NM_001142269.2:c.*3539G= NP_001135741.1:n.*3539G=
NM_001142269.3:c.*3539G= NP_001135741.1:n.*3539G=
NM_000821.7:c.*3539G= MANE Select NP_000812.2:n.*3539G=
NM_001142269.4:c.*3539G= NP_001135741.1:n.*3539G=
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