Canonical Allele Identifier: CA1266822737
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547889A= , CM000664.2:g.85547889A= GRCh38
NC_000002.11:g.85775012A= , CM000664.1:g.85775012A= GRCh37
NC_000002.10:g.85628523A= NCBI36
NG_011811.2:g.18646T=

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2045T= MANE Select ENSP00000233838.3:n.*2045T=
ENST00000233838.8:c.*2045T= ENSP00000233838.3:n.*2045T=
ENST00000465637.5:n.294T=
NM_000821.5:c.*2045T= NP_000812.2:n.*2045T=
NM_000821.6:c.*2045T= NP_000812.2:n.*2045T=
NM_001142269.2:c.*2045T= NP_001135741.1:n.*2045T=
NM_001142269.3:c.*2045T= NP_001135741.1:n.*2045T=
NM_000821.7:c.*2045T= MANE Select NP_000812.2:n.*2045T=
NM_001142269.4:c.*2045T= NP_001135741.1:n.*2045T=
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