Canonical Allele Identifier: CA196957963

Gene: ALDOB

Linked Data

• dbSNP Id: rs185271249
• gnomAD v3: 9-101429555-A-G
• gnomAD v4: 9-101429555-A-G
• MyVariant Identifiers: chr9:g.104191837A>G (hg19) ; chr9:g.101429555A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429555A>G , CM000671.2:g.101429555A>G	GRCh38
NC_000009.11:g.104191837A>G , CM000671.1:g.104191837A>G	GRCh37
NC_000009.10:g.103231658A>G	NCBI36
NG_012387.1:g.11226T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+200T>C MANE Select	ENSP00000497767.1:n.324+200T>C
ENST00000648064.1:c.324+200T>C	ENSP00000497990.1:n.324+200T>C
ENST00000648758.1:c.324+200T>C	ENSP00000497731.1:n.324+200T>C
ENST00000648906.1:n.694T>C
ENST00000649902.1:c.324+200T>C	ENSP00000497216.1:n.324+200T>C
ENST00000650613.1:n.600T>C
ENST00000374855.8:c.324+200T>C	ENSP00000363988.4:n.324+200T>C
ENST00000468981.3:n.67+254T>C
ENST00000616752.1:c.324+200T>C	ENSP00000481363.1:n.324+200T>C
NM_000035.3:c.324+200T>C	NP_000026.2:n.324+200T>C
NM_000035.4:c.324+200T>C MANE Select	NP_000026.2:n.324+200T>C