Canonical Allele Identifier: CA2014120497
Gene: GAPDH HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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