Canonical Allele Identifier: CA1868275210

Gene: ALDOB

Linked Data

• dbSNP Id: rs902219663

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421457G>C , CM000671.2:g.101421457G>C	GRCh38
NC_000009.11:g.104183739G>C , CM000671.1:g.104183739G>C	GRCh37
NC_000009.10:g.103223560G>C	NCBI36
NG_012387.1:g.19324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.*352C>G MANE Select	ENSP00000497767.1:n.*352C>G
ENST00000648064.1:c.*352C>G	ENSP00000497990.1:n.*352C>G
ENST00000374855.8:c.*352C>G	ENSP00000363988.4:n.*352C>G
NM_000035.3:c.*352C>G	NP_000026.2:n.*352C>G
NM_000035.4:c.*352C>G MANE Select	NP_000026.2:n.*352C>G