Canonical Allele Identifier: CA860757192

Gene: ABO

Linked Data

• dbSNP Id: rs112565602
• gnomAD v3: 9-133261647-G-T
• gnomAD v4: 9-133261647-G-T
• MyVariant Identifiers: chr9:g.136137050G>T (hg19) ; chr9:g.133261647G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261647G>T , CM000671.2:g.133261647G>T	GRCh38
NC_000009.11:g.136137050G>T , CM000671.1:g.136137050G>T	GRCh37
NC_000009.10:g.135126871G>T	NCBI36
NG_006669.1:g.16003C>A
NG_006669.2:g.18568C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.129-273C>A
ENST00000647353.1:n.54-10495C>A
ENST00000651471.1:n.134-273C>A
ENST00000679909.1:c.28+13515C>A	ENSP00000506089.1:n.28+13515C>A
ENST00000453660.3:n.111-273C>A
ENST00000538324.2:c.99-273C>A	ENSP00000483018.1:n.99-273C>A
ENST00000611156.4:c.99-273C>A	ENSP00000483265.1:n.99-273C>A
NM_020469.2:c.99-273C>A	NP_065202.2:n.99-273C>A
NM_020469.3:c.99-273C>A	NP_065202.2:n.99-273C>A