Canonical Allele Identifier: CA2691006170
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421403-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421403T>G , CM000671.2:g.101421403T>G GRCh38
NC_000009.11:g.104183685T>G , CM000671.1:g.104183685T>G GRCh37
NC_000009.10:g.103223506T>G NCBI36
NG_012387.1:g.19378A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*406A>C MANE Select ENSP00000497767.1:n.*406A>C
ENST00000374855.8:c.*406A>C ENSP00000363988.4:n.*406A>C
NM_000035.3:c.*406A>C NP_000026.2:n.*406A>C
NM_000035.4:c.*406A>C MANE Select NP_000026.2:n.*406A>C
Search 100 bp 5'
Search 100 bp 3'