Canonical Allele Identifier: CA1266822728
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547874A= , CM000664.2:g.85547874A= GRCh38
NC_000002.11:g.85774997A= , CM000664.1:g.85774997A= GRCh37
NC_000002.10:g.85628508A= NCBI36
NG_011811.2:g.18661T=

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2060T= MANE Select ENSP00000233838.3:n.*2060T=
ENST00000233838.8:c.*2060T= ENSP00000233838.3:n.*2060T=
ENST00000465637.5:n.309T=
NM_000821.5:c.*2060T= NP_000812.2:n.*2060T=
NM_000821.6:c.*2060T= NP_000812.2:n.*2060T=
NM_001142269.2:c.*2060T= NP_001135741.1:n.*2060T=
NM_001142269.3:c.*2060T= NP_001135741.1:n.*2060T=
NM_000821.7:c.*2060T= MANE Select NP_000812.2:n.*2060T=
NM_001142269.4:c.*2060T= NP_001135741.1:n.*2060T=
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