Canonical Allele Identifier: CA690978332
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs1416618617
MyVariant Identifiers: chr12:g.6643633T>A (hg19) chr12:g.6534467T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534467T>A , CM000674.2:g.6534467T>A GRCh38
NC_000012.11:g.6643633T>A , CM000674.1:g.6643633T>A GRCh37
NC_000012.10:g.6513894T>A NCBI36
NG_007073.2:g.4977T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-126T>A ENSP00000229239.5:n.-126T>A
NM_001289745.1:c.-218T>A NP_001276674.1:n.-218T>A
NM_002046.5:c.-126T>A NP_002037.2:n.-126T>A
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