Canonical Allele Identifier: CA466462142

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104187862C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425580C>A , CM000671.2:g.101425580C>A	GRCh38
NC_000009.11:g.104187862C>A , CM000671.1:g.104187862C>A	GRCh37
NC_000009.10:g.103227683C>A	NCBI36
NG_012387.1:g.15201G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.672G>T MANE Select	ENSP00000497767.1:p.Leu224=
ENST00000648064.1:c.672G>T	ENSP00000497990.1:p.Leu224=
ENST00000648758.1:c.672G>T	ENSP00000497731.1:p.Leu224=
ENST00000649902.1:c.672G>T	ENSP00000497216.1:p.Leu224=
ENST00000374855.8:c.672G>T	ENSP00000363988.4:p.Leu224=
ENST00000468981.3:n.199G>T
ENST00000616752.1:c.672G>T	ENSP00000481363.1:p.Leu224=
NM_000035.3:c.672G>T	NP_000026.2:p.Leu224=
NM_000035.4:c.672G>T MANE Select	NP_000026.2:p.Leu224=