Canonical Allele Identifier: CA196956776
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs764927361

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425494G>A , CM000671.2:g.101425494G>A GRCh38
NC_000009.11:g.104187776G>A , CM000671.1:g.104187776G>A GRCh37
NC_000009.10:g.103227597G>A NCBI36
NG_012387.1:g.15287C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.758C>T MANE Select ENSP00000497767.1:p.Thr253Ile
ENST00000648064.1:c.758C>T ENSP00000497990.1:p.Thr253Ile
ENST00000648758.1:c.758C>T ENSP00000497731.1:p.Thr253Ile
ENST00000649902.1:c.758C>T ENSP00000497216.1:p.Thr253Ile
ENST00000374855.8:c.758C>T ENSP00000363988.4:p.Thr253Ile
ENST00000616752.1:c.758C>T ENSP00000481363.1:p.Thr253Ile
NM_000035.3:c.758C>T NP_000026.2:p.Thr253Ile
NM_000035.4:c.758C>T MANE Select NP_000026.2:p.Thr253Ile