Canonical Allele Identifier: CA5161375
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs760375644
ExAC: 9:104184066 G / C
gnomAD v2: 9-104184066-G-C
gnomAD v3: 9-101421784-G-C
gnomAD v4: 9-101421784-G-C
MyVariant Identifiers: chr9:g.104184066G>C (hg19) chr9:g.101421784G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421784G>C , CM000671.2:g.101421784G>C GRCh38
NC_000009.11:g.104184066G>C , CM000671.1:g.104184066G>C GRCh37
NC_000009.10:g.103223887G>C NCBI36
NG_012387.1:g.18997C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*25C>G MANE Select ENSP00000497767.1:n.*25C>G
ENST00000648064.1:c.*25C>G ENSP00000497990.1:n.*25C>G
ENST00000648758.1:c.*25C>G ENSP00000497731.1:n.*25C>G
ENST00000374855.8:c.*25C>G ENSP00000363988.4:n.*25C>G
ENST00000616752.1:c.*132C>G ENSP00000481363.1:n.*132C>G
NM_000035.3:c.*25C>G NP_000026.2:n.*25C>G
NM_000035.4:c.*25C>G MANE Select NP_000026.2:n.*25C>G
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