Canonical Allele Identifier: CA2720569401

Gene: ABO

Linked Data

• dbSNP Id: rs2118956148

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260361del , CM000671.2:g.133260361del	GRCh38
NC_000009.11:g.136135764del , CM000671.1:g.136135764del	GRCh37
NC_000009.10:g.135125585del	NCBI36
NG_006669.1:g.17289del
NG_006669.2:g.19854del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.186-495del
ENST00000647353.1:n.54-9209del
ENST00000651471.1:n.191-495del
ENST00000679909.1:c.28+14801del	ENSP00000506089.1:n.28+14801del
ENST00000453660.3:n.168-495del
ENST00000538324.2:c.156-495del	ENSP00000483018.1:n.156-495del
ENST00000611156.4:c.156-495del	ENSP00000483265.1:n.156-495del
NM_020469.2:c.156-495del	NP_065202.2:n.156-495del
NM_020469.3:c.156-495del	NP_065202.2:n.156-495del