Canonical Allele Identifier: CA200766027

Gene: ABO

Linked Data

• dbSNP Id: rs906894108
• gnomAD v3: 9-133257318-CCA-C
• gnomAD v4: 9-133257318-CCA-C
• MyVariant Identifiers: chr9:g.136132706_136132707del (hg19) ; chr9:g.133257319_133257320del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257320_133257321del , CM000671.2:g.133257320_133257321del	GRCh38
NC_000009.11:g.136132707_136132708del , CM000671.1:g.136132707_136132708del	GRCh37
NC_000009.10:g.135122528_135122529del	NCBI36
NG_006669.1:g.20348_20349del
NG_006669.2:g.22896_22897del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.403+89_403+90del
ENST00000647353.1:n.54-6168_54-6167del
ENST00000651471.1:n.329+722_329+723del
ENST00000679909.1:c.28+17842_28+17843del	ENSP00000506089.1:n.28+17842_28+17843del
ENST00000453660.3:n.385+89_385+90del
ENST00000538324.2:c.371+89_371+90del	ENSP00000483018.1:n.371+89_371+90del
ENST00000611156.4:c.371+89_371+90del	ENSP00000483265.1:n.371+89_371+90del
NM_020469.2:c.374+89_374+90del	NP_065202.2:n.374+89_374+90del
NM_020469.3:c.374+89_374+90del	NP_065202.2:n.374+89_374+90del