Canonical Allele Identifier: CA196955615
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs966587043
MyVariant Identifiers: chr9:g.104183697C>G (hg19) chr9:g.101421415C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421415C>G , CM000671.2:g.101421415C>G GRCh38
NC_000009.11:g.104183697C>G , CM000671.1:g.104183697C>G GRCh37
NC_000009.10:g.103223518C>G NCBI36
NG_012387.1:g.19366G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*394G>C MANE Select ENSP00000497767.1:n.*394G>C
ENST00000374855.8:c.*394G>C ENSP00000363988.4:n.*394G>C
NM_000035.3:c.*394G>C NP_000026.2:n.*394G>C
NM_000035.4:c.*394G>C MANE Select NP_000026.2:n.*394G>C
Search 100 bp 5'
Search 100 bp 3'