Canonical Allele Identifier: CA2692330938

Gene: ABO

Linked Data

• gnomAD v4: 9-133258278-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258283del , CM000671.2:g.133258283del	GRCh38
NC_000009.11:g.136133674del , CM000671.1:g.136133674del	GRCh37
NC_000009.10:g.135123495del	NCBI36
NG_006669.1:g.19384del
NG_006669.2:g.21936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-147del
ENST00000647353.1:n.54-7127del
ENST00000651471.1:n.239-147del
ENST00000679909.1:c.28+16883del	ENSP00000506089.1:n.28+16883del
ENST00000453660.3:n.216-147del
ENST00000538324.2:c.204-147del	ENSP00000483018.1:n.204-147del
ENST00000611156.4:c.204-147del	ENSP00000483265.1:n.204-147del
NM_020469.2:c.204-147del	NP_065202.2:n.204-147del
NM_020469.3:c.204-147del	NP_065202.2:n.204-147del