Canonical Allele Identifier: CA1129725079

Gene: ABO

Linked Data

• gnomAD v3: 9-133274151-C-CAACCGAGAT
• gnomAD v4: 9-133274151-C-CAACCGAGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274151_133274152insAACCGAGAT , CM000671.2:g.133274151_133274152insAACCGAGAT	GRCh38
NC_000009.11:g.136149567_136149568insAACCGAGAT , CM000671.1:g.136149567_136149568insAACCGAGAT	GRCh37
NC_000009.10:g.135139388_135139389insAACCGAGAT	NCBI36
NG_006669.1:g.3483_3484insATCTCGGTT
NG_006669.2:g.6063_6064insATCTCGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.58+1010_58+1011insATCTCGGTT
ENST00000647353.1:n.53+1010_53+1011insATCTCGGTT
ENST00000651471.1:n.63+1810_63+1811insATCTCGGTT
ENST00000679909.1:c.28+1010_28+1011insATCTCGGTT	ENSP00000506089.1:n.28+1010_28+1011insATCTCGGTT
ENST00000453660.3:n.40+1010_40+1011insATCTCGGTT
ENST00000538324.2:c.28+1010_28+1011insATCTCGGTT	ENSP00000483018.1:n.28+1010_28+1011insATCTCGGTT
ENST00000611156.4:c.28+1010_28+1011insATCTCGGTT	ENSP00000483265.1:n.28+1010_28+1011insATCTCGGTT
NM_020469.2:c.28+1010_28+1011insATCTCGGTT	NP_065202.2:n.28+1010_28+1011insATCTCGGTT
NM_020469.3:c.28+1010_28+1011insATCTCGGTT	NP_065202.2:n.28+1010_28+1011insATCTCGGTT