Canonical Allele Identifier: CA6409372
Gene: GAPDH HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1136666

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534825C>G , CM000674.2:g.6534825C>G GRCh38
NC_000012.11:g.6643991C>G , CM000674.1:g.6643991C>G GRCh37
NC_000012.10:g.6514252C>G NCBI36
NG_007073.2:g.5335C>G

Transcript Alleles

HGVS Amino-acid change
NM_001289745.1:c.-8C>G VV NP_001276674.1:p.=
NM_001289746.1:c.-8C>G VV NP_001276675.1:p.=
NM_002046.5:c.-8C>G VV NP_002037.2:p.=
NM_001289745.2:c.-8C>G VV
NM_001357943.1:c.-8C>G VV NP_001344872.1:p.=
NM_002046.6:c.-8C>G VV
NR_152150.1:n.69C>G
NM_002046.7:c.-8C>G VV MANE Preferred
ENST00000229239.9:c.-8C>G ENSP00000229239.5:p.=
ENST00000396856.5:c.-260C>G ENSP00000380065.1:p.=
ENST00000396859.5:c.-8C>G ENSP00000380068.1:p.=
ENST00000396861.5:c.-8C>G ENSP00000380070.1:p.=
ENST00000466525.1:n.34C>G
ENST00000466588.5:n.72C>G
ENST00000474249.5:n.45C>G
ENST00000492719.5:n.53C>G
ENST00000496049.1:n.74C>G