Canonical Allele Identifier: CA1868278899

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831108983

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425290G>A , CM000671.2:g.101425290G>A	GRCh38
NC_000009.11:g.104187572G>A , CM000671.1:g.104187572G>A	GRCh37
NC_000009.10:g.103227393G>A	NCBI36
NG_012387.1:g.15491C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.799+163C>T MANE Select	ENSP00000497767.1:n.799+163C>T
ENST00000648064.1:c.799+163C>T	ENSP00000497990.1:n.799+163C>T
ENST00000648758.1:c.799+163C>T	ENSP00000497731.1:n.799+163C>T
ENST00000649902.1:c.799+163C>T	ENSP00000497216.1:n.799+163C>T
ENST00000374855.8:c.799+163C>T	ENSP00000363988.4:n.799+163C>T
ENST00000616752.1:c.799+163C>T	ENSP00000481363.1:n.799+163C>T
NM_000035.3:c.799+163C>T	NP_000026.2:n.799+163C>T
NM_000035.4:c.799+163C>T MANE Select	NP_000026.2:n.799+163C>T