Canonical Allele Identifier: CA2692330788

Gene: ABO

Linked Data

• gnomAD v4: 9-133258037-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258037A>T , CM000671.2:g.133258037A>T	GRCh38
NC_000009.11:g.136133427A>T , CM000671.1:g.136133427A>T	GRCh37
NC_000009.10:g.135123248A>T	NCBI36
NG_006669.1:g.19627T>A
NG_006669.2:g.22178T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+60T>A
ENST00000647353.1:n.54-6885T>A
ENST00000651471.1:n.329+5T>A
ENST00000679909.1:c.28+17125T>A	ENSP00000506089.1:n.28+17125T>A
ENST00000453660.3:n.251+60T>A
ENST00000538324.2:c.239+60T>A	ENSP00000483018.1:n.239+60T>A
ENST00000611156.4:c.239+60T>A	ENSP00000483265.1:n.239+60T>A
NM_020469.2:c.239+60T>A	NP_065202.2:n.239+60T>A
NM_020469.3:c.239+60T>A	NP_065202.2:n.239+60T>A