Canonical Allele Identifier: CA1129717017

Gene: ABO

Linked Data

• gnomAD v3: 9-133260062-C-CG
• gnomAD v4: 9-133260062-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260062_133260063insG , CM000671.2:g.133260062_133260063insG	GRCh38
NC_000009.11:g.136135466_136135467insG , CM000671.1:g.136135466_136135467insG	GRCh37
NC_000009.10:g.135125287_135125288insG	NCBI36
NG_006669.1:g.17587_17588insC
NG_006669.2:g.20152_20153insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.186-197_186-196insC
ENST00000647353.1:n.54-8911_54-8910insC
ENST00000651471.1:n.191-197_191-196insC
ENST00000679909.1:c.28+15099_28+15100insC	ENSP00000506089.1:n.28+15099_28+15100insC
ENST00000453660.3:n.168-197_168-196insC
ENST00000538324.2:c.156-197_156-196insC	ENSP00000483018.1:n.156-197_156-196insC
ENST00000611156.4:c.156-197_156-196insC	ENSP00000483265.1:n.156-197_156-196insC
NM_020469.2:c.156-197_156-196insC	NP_065202.2:n.156-197_156-196insC
NM_020469.3:c.156-197_156-196insC	NP_065202.2:n.156-197_156-196insC