Canonical Allele Identifier: CA2659853413
Gene: GGCX HGNC NCBI

Linked Data

gnomAD v4: 2-85547901-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547901T>C , CM000664.2:g.85547901T>C GRCh38
NC_000002.11:g.85775024T>C , CM000664.1:g.85775024T>C GRCh37
NC_000002.10:g.85628535T>C NCBI36
NG_011811.2:g.18634A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2033A>G MANE Select ENSP00000233838.3:n.*2033A>G
ENST00000233838.8:c.*2033A>G ENSP00000233838.3:n.*2033A>G
ENST00000465637.5:n.282A>G
NM_000821.5:c.*2033A>G NP_000812.2:n.*2033A>G
NM_000821.6:c.*2033A>G NP_000812.2:n.*2033A>G
NM_001142269.2:c.*2033A>G NP_001135741.1:n.*2033A>G
NM_001142269.3:c.*2033A>G NP_001135741.1:n.*2033A>G
NM_000821.7:c.*2033A>G MANE Select NP_000812.2:n.*2033A>G
NM_001142269.4:c.*2033A>G NP_001135741.1:n.*2033A>G
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