Canonical Allele Identifier: CA1868275345
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1588168853

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421622C>A , CM000671.2:g.101421622C>A GRCh38
NC_000009.11:g.104183904C>A , CM000671.1:g.104183904C>A GRCh37
NC_000009.10:g.103223725C>A NCBI36
NG_012387.1:g.19159G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*187G>T MANE Select ENSP00000497767.1:n.*187G>T
ENST00000648064.1:c.*187G>T ENSP00000497990.1:n.*187G>T
ENST00000374855.8:c.*187G>T ENSP00000363988.4:n.*187G>T
ENST00000616752.1:c.*294G>T ENSP00000481363.1:n.*294G>T
NM_000035.3:c.*187G>T NP_000026.2:n.*187G>T
NM_000035.4:c.*187G>T MANE Select NP_000026.2:n.*187G>T