Canonical Allele Identifier: CA1129716170

Gene: ABO

Linked Data

• dbSNP Id: rs1834630335

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257791_133257792del , CM000671.2:g.133257791_133257792del	GRCh38
NC_000009.11:g.136133178_136133179del , CM000671.1:g.136133178_136133179del	GRCh37
NC_000009.10:g.135122999_135123000del	NCBI36
NG_006669.1:g.19875_19876del
NG_006669.2:g.22423_22424del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.270-250_270-249del
ENST00000647353.1:n.54-6640_54-6639del
ENST00000651471.1:n.329+250_329+251del
ENST00000679909.1:c.28+17370_28+17371del	ENSP00000506089.1:n.28+17370_28+17371del
ENST00000453660.3:n.252-250_252-249del
ENST00000538324.2:c.240-250_240-249del	ENSP00000483018.1:n.240-250_240-249del
ENST00000611156.4:c.240-250_240-249del	ENSP00000483265.1:n.240-250_240-249del
NM_020469.2:c.240-250_240-249del	NP_065202.2:n.240-250_240-249del
NM_020469.3:c.240-250_240-249del	NP_065202.2:n.240-250_240-249del