Canonical Allele Identifier: CA2014120483
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs1946411641
gnomAD v4: 12-6534464-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534464G>A , CM000674.2:g.6534464G>A GRCh38
NC_000012.11:g.6643630G>A , CM000674.1:g.6643630G>A GRCh37
NC_000012.10:g.6513891G>A NCBI36
NG_007073.2:g.4974G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-129G>A ENSP00000229239.5:n.-129G>A
NM_001289745.1:c.-221G>A NP_001276674.1:n.-221G>A
NM_002046.5:c.-129G>A NP_002037.2:n.-129G>A
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