Canonical Allele Identifier: CA2720239580

Gene: ALDOB

Linked Data

• dbSNP Id: rs2118331876

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421515G>C , CM000671.2:g.101421515G>C	GRCh38
NC_000009.11:g.104183797G>C , CM000671.1:g.104183797G>C	GRCh37
NC_000009.10:g.103223618G>C	NCBI36
NG_012387.1:g.19266C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.*294C>G MANE Select	ENSP00000497767.1:n.*294C>G
ENST00000648064.1:c.*294C>G	ENSP00000497990.1:n.*294C>G
ENST00000374855.8:c.*294C>G	ENSP00000363988.4:n.*294C>G
NM_000035.3:c.*294C>G	NP_000026.2:n.*294C>G
NM_000035.4:c.*294C>G MANE Select	NP_000026.2:n.*294C>G