Canonical Allele Identifier: CA466461841
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1194552507
gnomAD v2: 9-104184169-G-A
gnomAD v3: 9-101421887-G-A
gnomAD v4: 9-101421887-G-A
MyVariant Identifiers: chr9:g.104184169G>A (hg19) chr9:g.101421887G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421887G>A , CM000671.2:g.101421887G>A GRCh38
NC_000009.11:g.104184169G>A , CM000671.1:g.104184169G>A GRCh37
NC_000009.10:g.103223990G>A NCBI36
NG_012387.1:g.18894C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.1017C>T MANE Select ENSP00000497767.1:p.Ala339=
ENST00000648064.1:c.1017C>T ENSP00000497990.1:p.Ala339=
ENST00000648758.1:c.1017C>T ENSP00000497731.1:p.Ala339=
ENST00000374855.8:c.1017C>T ENSP00000363988.4:p.Ala339=
ENST00000616752.1:c.*29C>T ENSP00000481363.1:n.*29C>T
NM_000035.3:c.1017C>T NP_000026.2:p.Ala339=
NM_000035.4:c.1017C>T MANE Select NP_000026.2:p.Ala339=
Search 100 bp 5'
Search 100 bp 3'