Canonical Allele Identifier: CA857728380
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1332946756
MyVariant Identifiers: chr9:g.104183789C>G (hg19) chr9:g.101421507C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421507C>G , CM000671.2:g.101421507C>G GRCh38
NC_000009.11:g.104183789C>G , CM000671.1:g.104183789C>G GRCh37
NC_000009.10:g.103223610C>G NCBI36
NG_012387.1:g.19274G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*302G>C MANE Select ENSP00000497767.1:n.*302G>C
ENST00000648064.1:c.*302G>C ENSP00000497990.1:n.*302G>C
ENST00000374855.8:c.*302G>C ENSP00000363988.4:n.*302G>C
NM_000035.3:c.*302G>C NP_000026.2:n.*302G>C
NM_000035.4:c.*302G>C MANE Select NP_000026.2:n.*302G>C
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