Canonical Allele Identifier: CA232399779

Gene: GAPDH

Linked Data

• dbSNP Id: rs947590041
• gnomAD v3: 12-6534521-T-G
• gnomAD v4: 12-6534521-T-G
• MyVariant Identifiers: chr12:g.6643687T>G (hg19) ; chr12:g.6534521T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534521T>G , CM000674.2:g.6534521T>G	GRCh38
NC_000012.11:g.6643687T>G , CM000674.1:g.6643687T>G	GRCh37
NC_000012.10:g.6513948T>G	NCBI36
NG_007073.2:g.5031T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-72T>G MANE Select	ENSP00000229239.5:n.-72T>G
ENST00000229239.9:c.-72T>G	ENSP00000229239.5:n.-72T>G
ENST00000496049.1:n.10T>G
NM_001289745.1:c.-164T>G	NP_001276674.1:n.-164T>G
NM_002046.5:c.-72T>G	NP_002037.2:n.-72T>G
NM_001289745.2:c.-164T>G	NP_001276674.1:n.-164T>G
NM_001357943.1:c.-72T>G	NP_001344872.1:n.-72T>G
NM_002046.6:c.-72T>G	NP_002037.2:n.-72T>G
NR_152150.1:n.5T>G
NM_002046.7:c.-72T>G MANE Select	NP_002037.2:n.-72T>G
NM_001289745.3:c.-164T>G	NP_001276674.1:n.-164T>G
NM_001289746.2:c.-312T>G	NP_001276675.1:n.-312T>G
NM_001357943.2:c.-72T>G	NP_001344872.1:n.-72T>G
NR_152150.2:n.5T>G