Canonical Allele Identifier: CA2014120500
Gene: GAPDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534482G= , CM000674.2:g.6534482G= GRCh38
NC_000012.11:g.6643648G= , CM000674.1:g.6643648G= GRCh37
NC_000012.10:g.6513909G= NCBI36
NG_007073.2:g.4992G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-111G= ENSP00000229239.5:n.-111G=
NM_001289745.1:c.-203G= NP_001276674.1:n.-203G=
NM_002046.5:c.-111G= NP_002037.2:n.-111G=