Canonical Allele Identifier: CA375682255

Gene: ABO

Linked Data

• dbSNP Id: rs1834556985
• gnomAD v3: 9-133255645-C-T
• gnomAD v4: 9-133255645-C-T
• MyVariant Identifiers: chr9:g.136131032C>T (hg19) ; chr9:g.133255645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255645C>T , CM000671.2:g.133255645C>T	GRCh38
NC_000009.11:g.136131032C>T , CM000671.1:g.136131032C>T	GRCh37
NC_000009.10:g.135120853C>T	NCBI36
NG_006669.1:g.22023G>A
NG_006669.2:g.24571G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1115G>A
ENST00000647353.1:n.54-4493G>A
ENST00000679909.1:c.28+19517G>A	ENSP00000506089.1:n.28+19517G>A
ENST00000453660.3:n.1097G>A
ENST00000538324.2:c.1079G>A	ENSP00000483018.1:p.Gly360Glu
ENST00000611156.4:c.*21G>A	ENSP00000483265.1:n.*21G>A
NM_020469.2:c.*21G>A	NP_065202.2:n.*21G>A
NM_020469.3:c.*21G>A	NP_065202.2:n.*21G>A