Canonical Allele Identifier: CA232399714
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs1003996379
gnomAD v2: 12-6643648-G-A
gnomAD v3: 12-6534482-G-A
gnomAD v4: 12-6534482-G-A
MyVariant Identifiers: chr12:g.6643648G>A (hg19) chr12:g.6534482G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534482G>A , CM000674.2:g.6534482G>A GRCh38
NC_000012.11:g.6643648G>A , CM000674.1:g.6643648G>A GRCh37
NC_000012.10:g.6513909G>A NCBI36
NG_007073.2:g.4992G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-111G>A ENSP00000229239.5:n.-111G>A
NM_001289745.1:c.-203G>A NP_001276674.1:n.-203G>A
NM_002046.5:c.-111G>A NP_002037.2:n.-111G>A
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