Canonical Allele Identifier: CA196957749

Gene: ALDOB

Linked Data

• dbSNP Id: rs143271050
• MyVariant Identifiers: chr9:g.101428749G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101428749G>A , CM000671.2:g.101428749G>A	GRCh38
NC_000009.11:g.104191031G>A , CM000671.1:g.104191031G>A	GRCh37
NC_000009.10:g.103230852G>A	NCBI36
NG_012387.1:g.12032C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.325-226C>T MANE Select	ENSP00000497767.1:n.325-226C>T
ENST00000648064.1:c.325-226C>T	ENSP00000497990.1:n.325-226C>T
ENST00000648758.1:c.325-226C>T	ENSP00000497731.1:n.325-226C>T
ENST00000649902.1:c.325-226C>T	ENSP00000497216.1:n.325-226C>T
ENST00000374855.8:c.325-226C>T	ENSP00000363988.4:n.325-226C>T
ENST00000468981.3:n.67+1060C>T
ENST00000616752.1:c.325-226C>T	ENSP00000481363.1:n.325-226C>T
NM_000035.3:c.325-226C>T	NP_000026.2:n.325-226C>T
NM_000035.4:c.325-226C>T MANE Select	NP_000026.2:n.325-226C>T