Canonical Allele Identifier: CA2499219516
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1065865
ClinVar RCV Id: RCV001376719

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425219_101426793del , CM000671.2:g.101425219_101426793del GRCh38
NC_000009.11:g.104187501_104189075del , CM000671.1:g.104187501_104189075del GRCh37
NC_000009.10:g.103227322_103228896del NCBI36
NG_012387.1:g.13990_15564del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.541-153_800-175del
ENST00000648064.1:c.541-153_800-175del
ENST00000648758.1:c.541-153_800-175del
ENST00000649902.1:c.541-153_800-175del
ENST00000374855.8:c.541-153_800-175del
ENST00000616752.1:c.541-153_800-175del
NM_000035.3:c.541-153_800-175del
NM_000035.4:c.541-153_800-175del