Canonical Allele Identifier: CA232399718
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs1033816878
gnomAD v3: 12-6534501-C-T
gnomAD v4: 12-6534501-C-T
MyVariant Identifiers: chr12:g.6643667C>T (hg19) chr12:g.6534501C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534501C>T , CM000674.2:g.6534501C>T GRCh38
NC_000012.11:g.6643667C>T , CM000674.1:g.6643667C>T GRCh37
NC_000012.10:g.6513928C>T NCBI36
NG_007073.2:g.5011C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-92C>T ENSP00000229239.5:n.-92C>T
NM_001289745.1:c.-184C>T NP_001276674.1:n.-184C>T
NM_002046.5:c.-92C>T NP_002037.2:n.-92C>T
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