Canonical Allele Identifier: CA232399674
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs960441787
gnomAD v3: 12-6534470-C-T
gnomAD v4: 12-6534470-C-T
MyVariant Identifiers: chr12:g.6643636C>T (hg19) chr12:g.6534470C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534470C>T , CM000674.2:g.6534470C>T GRCh38
NC_000012.11:g.6643636C>T , CM000674.1:g.6643636C>T GRCh37
NC_000012.10:g.6513897C>T NCBI36
NG_007073.2:g.4980C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-123C>T ENSP00000229239.5:n.-123C>T
NM_001289745.1:c.-215C>T NP_001276674.1:n.-215C>T
NM_002046.5:c.-123C>T NP_002037.2:n.-123C>T
Search 100 bp 5'
Search 100 bp 3'