Canonical Allele Identifier: CA1882578694

Gene: ABO

Linked Data

• dbSNP Id: rs908134529
• gnomAD v4: 9-133255435-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255445_133255446dup , CM000671.2:g.133255445_133255446dup	GRCh38
NC_000009.11:g.136130832_136130833dup , CM000671.1:g.136130832_136130833dup	GRCh37
NC_000009.10:g.135120653_135120654dup	NCBI36
NG_006669.1:g.22231_22232dup
NG_006669.2:g.24779_24780dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1323_1324dup
ENST00000647353.1:n.54-4285_54-4284dup
ENST00000679909.1:c.28+19725_28+19726dup	ENSP00000506089.1:n.28+19725_28+19726dup
ENST00000453660.3:n.1305_1306dup
ENST00000611156.4:c.*229_*230dup	ENSP00000483265.1:n.*229_*230dup
NM_020469.2:c.*229_*230dup	NP_065202.2:n.*229_*230dup
NM_020469.3:c.*229_*230dup	NP_065202.2:n.*229_*230dup