Canonical Allele Identifier: CA2691006343
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421689-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421689T>G , CM000671.2:g.101421689T>G GRCh38
NC_000009.11:g.104183971T>G , CM000671.1:g.104183971T>G GRCh37
NC_000009.10:g.103223792T>G NCBI36
NG_012387.1:g.19092A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*120A>C MANE Select ENSP00000497767.1:n.*120A>C
ENST00000648064.1:c.*120A>C ENSP00000497990.1:n.*120A>C
ENST00000648758.1:c.*120A>C ENSP00000497731.1:n.*120A>C
ENST00000374855.8:c.*120A>C ENSP00000363988.4:n.*120A>C
ENST00000616752.1:c.*227A>C ENSP00000481363.1:n.*227A>C
NM_000035.3:c.*120A>C NP_000026.2:n.*120A>C
NM_000035.4:c.*120A>C MANE Select NP_000026.2:n.*120A>C
Search 100 bp 5'
Search 100 bp 3'