Canonical Allele Identifier: CA690978347
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs1393052222
MyVariant Identifiers: chr12:g.6643673C>T (hg19) chr12:g.6534507C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534507C>T , CM000674.2:g.6534507C>T GRCh38
NC_000012.11:g.6643673C>T , CM000674.1:g.6643673C>T GRCh37
NC_000012.10:g.6513934C>T NCBI36
NG_007073.2:g.5017C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-86C>T ENSP00000229239.5:n.-86C>T
NM_001289745.1:c.-178C>T NP_001276674.1:n.-178C>T
NM_002046.5:c.-86C>T NP_002037.2:n.-86C>T
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