Canonical Allele Identifier: CA1882578428

Gene: ABO

Linked Data

• dbSNP Id: rs1823508923

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255334_133255335del , CM000671.2:g.133255334_133255335del	GRCh38
NC_000009.11:g.136130721_136130722del , CM000671.1:g.136130721_136130722del	GRCh37
NC_000009.10:g.135120542_135120543del	NCBI36
NG_006669.1:g.22334_22335del
NG_006669.2:g.24882_24883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1426_1427del
ENST00000647353.1:n.54-4182_54-4181del
ENST00000679909.1:c.28+19828_28+19829del	ENSP00000506089.1:n.28+19828_28+19829del
ENST00000453660.3:n.1408_1409del
ENST00000611156.4:c.*332_*333del	ENSP00000483265.1:n.*332_*333del
NM_020469.2:c.*332_*333del	NP_065202.2:n.*332_*333del
NM_020469.3:c.*332_*333del	NP_065202.2:n.*332_*333del