Canonical Allele Identifier: CA690978336
Gene: GAPDH HGNC NCBI

Linked Data

dbSNP Id: rs1185313071
gnomAD v3: 12-6534469-C-G
gnomAD v4: 12-6534469-C-G
MyVariant Identifiers: chr12:g.6643635C>G (hg19) chr12:g.6534469C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534469C>G , CM000674.2:g.6534469C>G GRCh38
NC_000012.11:g.6643635C>G , CM000674.1:g.6643635C>G GRCh37
NC_000012.10:g.6513896C>G NCBI36
NG_007073.2:g.4979C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.9:c.-124C>G ENSP00000229239.5:n.-124C>G
NM_001289745.1:c.-216C>G NP_001276674.1:n.-216C>G
NM_002046.5:c.-124C>G NP_002037.2:n.-124C>G
Search 100 bp 5'
Search 100 bp 3'