Canonical Allele Identifier: CA1868275316
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831047229
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421587T>G , CM000671.2:g.101421587T>G GRCh38
NC_000009.11:g.104183869T>G , CM000671.1:g.104183869T>G GRCh37
NC_000009.10:g.103223690T>G NCBI36
NG_012387.1:g.19194A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*222A>C MANE Select ENSP00000497767.1:n.*222A>C
ENST00000648064.1:c.*222A>C ENSP00000497990.1:n.*222A>C
ENST00000374855.8:c.*222A>C ENSP00000363988.4:n.*222A>C
ENST00000616752.1:c.*329A>C ENSP00000481363.1:n.*329A>C
NM_000035.3:c.*222A>C NP_000026.2:n.*222A>C
NM_000035.4:c.*222A>C MANE Select NP_000026.2:n.*222A>C
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