Canonical Allele Identifier: CA375682217

Gene: ABO

Linked Data

• gnomAD v4: 9-133255622-G-T
• MyVariant Identifiers: chr9:g.136131009G>T (hg19) ; chr9:g.133255622G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255622G>T , CM000671.2:g.133255622G>T	GRCh38
NC_000009.11:g.136131009G>T , CM000671.1:g.136131009G>T	GRCh37
NC_000009.10:g.135120830G>T	NCBI36
NG_006669.1:g.22046C>A
NG_006669.2:g.24594C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1138C>A
ENST00000647353.1:n.54-4470C>A
ENST00000679909.1:c.28+19540C>A	ENSP00000506089.1:n.28+19540C>A
ENST00000453660.3:n.1120C>A
ENST00000538324.2:c.1102C>A	ENSP00000483018.1:p.Pro368Thr
ENST00000611156.4:c.*44C>A	ENSP00000483265.1:n.*44C>A
NM_020469.2:c.*44C>A	NP_065202.2:n.*44C>A
NM_020469.3:c.*44C>A	NP_065202.2:n.*44C>A