Canonical Allele Identifier: CA857728375
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1377257062
gnomAD v3: 9-101421500-AGTT-A
gnomAD v4: 9-101421500-AGTT-A
MyVariant Identifiers: chr9:g.104183783_104183785del (hg19) chr9:g.101421501_101421503del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421504_101421506del , CM000671.2:g.101421504_101421506del GRCh38
NC_000009.11:g.104183786_104183788del , CM000671.1:g.104183786_104183788del GRCh37
NC_000009.10:g.103223607_103223609del NCBI36
NG_012387.1:g.19278_19280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*306_*308del MANE Select ENSP00000497767.1:n.*306_*308del
ENST00000648064.1:c.*306_*308del ENSP00000497990.1:n.*306_*308del
ENST00000374855.8:c.*306_*308del ENSP00000363988.4:n.*306_*308del
NM_000035.3:c.*306_*308del NP_000026.2:n.*306_*308del
NM_000035.4:c.*306_*308del MANE Select NP_000026.2:n.*306_*308del
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