Canonical Allele Identifier: CA200764977

Gene: ABO

Linked Data

• dbSNP Id: rs386739123

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255488_133255493delinsAACGGT , CM000671.2:g.133255488_133255493delinsAACGGT	GRCh38
NC_000009.11:g.136130875_136130880delinsAACGGT , CM000671.1:g.136130875_136130880delinsAACGGT	GRCh37
NC_000009.10:g.135120696_135120701delinsAACGGT	NCBI36
NG_006669.1:g.22175_22180delinsACCGTT
NG_006669.2:g.24723_24728delinsACCGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1267_1272delinsACCGTT
ENST00000647353.1:n.54-4341_54-4336delinsACCGTT
ENST00000679909.1:c.28+19669_28+19674delinsACCGTT	ENSP00000506089.1:n.28+19669_28+19674delinsACCGTT
ENST00000453660.3:n.1249_1254delinsACCGTT
ENST00000611156.4:c.*173_*178delinsACCGTT	ENSP00000483265.1:n.*173_*178delinsACCGTT
NM_020469.2:c.*173_*178delinsACCGTT	NP_065202.2:n.*173_*178delinsACCGTT
NM_020469.3:c.*173_*178delinsACCGTT	NP_065202.2:n.*173_*178delinsACCGTT