Canonical Allele Identifier: CA196955650
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs762406910
gnomAD v4: 9-101421518-G-A
MyVariant Identifiers: chr9:g.104183800G>A (hg19) chr9:g.101421518G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421518G>A , CM000671.2:g.101421518G>A GRCh38
NC_000009.11:g.104183800G>A , CM000671.1:g.104183800G>A GRCh37
NC_000009.10:g.103223621G>A NCBI36
NG_012387.1:g.19263C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*291C>T MANE Select ENSP00000497767.1:n.*291C>T
ENST00000648064.1:c.*291C>T ENSP00000497990.1:n.*291C>T
ENST00000374855.8:c.*291C>T ENSP00000363988.4:n.*291C>T
NM_000035.3:c.*291C>T NP_000026.2:n.*291C>T
NM_000035.4:c.*291C>T MANE Select NP_000026.2:n.*291C>T
Search 100 bp 5'
Search 100 bp 3'