Canonical Allele Identifier: CA2014120498
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs1946412213
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534481C>A , CM000674.2:g.6534481C>A GRCh38
NC_000012.11:g.6643647C>A , CM000674.1:g.6643647C>A GRCh37
NC_000012.10:g.6513908C>A NCBI36
NG_007073.2:g.4991C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-112C>A ENSP00000229239.5:n.-112C>A
NM_001289745.1:c.-204C>A NP_001276674.1:n.-204C>A
NM_002046.5:c.-112C>A NP_002037.2:n.-112C>A
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