Canonical Allele Identifier: CA2617278373
Gene: GAPDH HGNC NCBI

Linked Data

gnomAD v4: 12-6534478-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534478C>A , CM000674.2:g.6534478C>A GRCh38
NC_000012.11:g.6643644C>A , CM000674.1:g.6643644C>A GRCh37
NC_000012.10:g.6513905C>A NCBI36
NG_007073.2:g.4988C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-115C>A ENSP00000229239.5:n.-115C>A
NM_001289745.1:c.-207C>A NP_001276674.1:n.-207C>A
NM_002046.5:c.-115C>A NP_002037.2:n.-115C>A