Canonical Allele Identifier: CA2617278396
Gene: GAPDH HGNC NCBI

Linked Data

gnomAD v4: 12-6534498-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534498G>T , CM000674.2:g.6534498G>T GRCh38
NC_000012.11:g.6643664G>T , CM000674.1:g.6643664G>T GRCh37
NC_000012.10:g.6513925G>T NCBI36
NG_007073.2:g.5008G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-95G>T ENSP00000229239.5:n.-95G>T
NM_001289745.1:c.-187G>T NP_001276674.1:n.-187G>T
NM_002046.5:c.-95G>T NP_002037.2:n.-95G>T
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