Canonical Allele Identifier: CA2014120485
Gene: GAPDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534467T= , CM000674.2:g.6534467T= GRCh38
NC_000012.11:g.6643633T= , CM000674.1:g.6643633T= GRCh37
NC_000012.10:g.6513894T= NCBI36
NG_007073.2:g.4977T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-126T= ENSP00000229239.5:n.-126T=
NM_001289745.1:c.-218T= NP_001276674.1:n.-218T=
NM_002046.5:c.-126T= NP_002037.2:n.-126T=