Canonical Allele Identifier: CA2617278358
Gene: GAPDH HGNC NCBI

Linked Data

gnomAD v4: 12-6534462-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534462C>G , CM000674.2:g.6534462C>G GRCh38
NC_000012.11:g.6643628C>G , CM000674.1:g.6643628C>G GRCh37
NC_000012.10:g.6513889C>G NCBI36
NG_007073.2:g.4972C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-131C>G ENSP00000229239.5:n.-131C>G
NM_001289745.1:c.-223C>G NP_001276674.1:n.-223C>G
NM_002046.5:c.-131C>G NP_002037.2:n.-131C>G
Search 100 bp 5'
Search 100 bp 3'