Canonical Allele Identifier: CA2617278376
Gene: GAPDH HGNC NCBI

Linked Data

gnomAD v4: 12-6534479-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534479C>G , CM000674.2:g.6534479C>G GRCh38
NC_000012.11:g.6643645C>G , CM000674.1:g.6643645C>G GRCh37
NC_000012.10:g.6513906C>G NCBI36
NG_007073.2:g.4989C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-114C>G ENSP00000229239.5:n.-114C>G
NM_001289745.1:c.-206C>G NP_001276674.1:n.-206C>G
NM_002046.5:c.-114C>G NP_002037.2:n.-114C>G
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