Canonical Allele Identifier: CA5161504
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs766027880
ExAC: 9:104187855 T / A
gnomAD v2: 9-104187855-T-A
gnomAD v3: 9-101425573-T-A
gnomAD v4: 9-101425573-T-A
MyVariant Identifiers: chr9:g.104187855T>A (hg19) chr9:g.101425573T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425573T>A , CM000671.2:g.101425573T>A GRCh38
NC_000009.11:g.104187855T>A , CM000671.1:g.104187855T>A GRCh37
NC_000009.10:g.103227676T>A NCBI36
NG_012387.1:g.15208A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.679A>T MANE Select ENSP00000497767.1:p.Thr227Ser
ENST00000648064.1:c.679A>T ENSP00000497990.1:p.Thr227Ser
ENST00000648758.1:c.679A>T ENSP00000497731.1:p.Thr227Ser
ENST00000649902.1:c.679A>T ENSP00000497216.1:p.Thr227Ser
ENST00000374855.8:c.679A>T ENSP00000363988.4:p.Thr227Ser
ENST00000468981.3:n.206A>T
ENST00000616752.1:c.679A>T ENSP00000481363.1:p.Thr227Ser
NM_000035.3:c.679A>T NP_000026.2:p.Thr227Ser
NM_000035.4:c.679A>T MANE Select NP_000026.2:p.Thr227Ser
Search 100 bp 5'
Search 100 bp 3'