Canonical Allele Identifier: CA2617278355
Gene: GAPDH HGNC NCBI

Linked Data

gnomAD v4: 12-6534459-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534459T>C , CM000674.2:g.6534459T>C GRCh38
NC_000012.11:g.6643625T>C , CM000674.1:g.6643625T>C GRCh37
NC_000012.10:g.6513886T>C NCBI36
NG_007073.2:g.4969T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-134T>C ENSP00000229239.5:n.-134T>C
NM_001289745.1:c.-226T>C NP_001276674.1:n.-226T>C
NM_002046.5:c.-134T>C NP_002037.2:n.-134T>C
Search 100 bp 5'
Search 100 bp 3'