Canonical Allele Identifier: CA2617278361
Gene: GAPDH HGNC NCBI

Linked Data

gnomAD v4: 12-6534466-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534466C>T , CM000674.2:g.6534466C>T GRCh38
NC_000012.11:g.6643632C>T , CM000674.1:g.6643632C>T GRCh37
NC_000012.10:g.6513893C>T NCBI36
NG_007073.2:g.4976C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-127C>T ENSP00000229239.5:n.-127C>T
NM_001289745.1:c.-219C>T NP_001276674.1:n.-219C>T
NM_002046.5:c.-127C>T NP_002037.2:n.-127C>T
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