Canonical Allele Identifier: CA1882583479

Gene: ABO

Linked Data

• dbSNP Id: rs1834641426

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258402_133258406del , CM000671.2:g.133258402_133258406del	GRCh38
NC_000009.11:g.136133793_136133797del , CM000671.1:g.136133793_136133797del	GRCh37
NC_000009.10:g.135123614_135123618del	NCBI36
NG_006669.1:g.19261_19265del
NG_006669.2:g.21813_21817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-270_234-266del
ENST00000647353.1:n.54-7250_54-7246del
ENST00000651471.1:n.239-270_239-266del
ENST00000679909.1:c.28+16760_28+16764del	ENSP00000506089.1:n.28+16760_28+16764del
ENST00000453660.3:n.216-270_216-266del
ENST00000538324.2:c.204-270_204-266del	ENSP00000483018.1:n.204-270_204-266del
ENST00000611156.4:c.204-270_204-266del	ENSP00000483265.1:n.204-270_204-266del
NM_020469.2:c.204-270_204-266del	NP_065202.2:n.204-270_204-266del
NM_020469.3:c.204-270_204-266del	NP_065202.2:n.204-270_204-266del