Canonical Allele Identifier: CA200765005

Gene: ABO

Linked Data

• dbSNP Id: rs947820967
• gnomAD v3: 9-133255515-G-GGC
• gnomAD v4: 9-133255515-G-GGC
• MyVariant Identifiers: chr9:g.136130902_136130903insGC (hg19) ; chr9:g.133255515_133255516insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255516_133255517insCG , CM000671.2:g.133255516_133255517insCG	GRCh38
NC_000009.11:g.136130903_136130904insCG , CM000671.1:g.136130903_136130904insCG	GRCh37
NC_000009.10:g.135120724_135120725insCG	NCBI36
NG_006669.1:g.22152_22153insGC
NG_006669.2:g.24700_24701insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1244_1245insGC
ENST00000647353.1:n.54-4364_54-4363insGC
ENST00000679909.1:c.28+19646_28+19647insGC	ENSP00000506089.1:n.28+19646_28+19647insGC
ENST00000453660.3:n.1226_1227insGC
ENST00000611156.4:c.*150_*151insGC	ENSP00000483265.1:n.*150_*151insGC
NM_020469.2:c.*150_*151insGC	NP_065202.2:n.*150_*151insGC
NM_020469.3:c.*150_*151insGC	NP_065202.2:n.*150_*151insGC