Canonical Allele Identifier: CA375685587

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131432A>T (hg19) ; chr9:g.133256045A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256045A>T , CM000671.2:g.133256045A>T	GRCh38
NC_000009.11:g.136131432A>T , CM000671.1:g.136131432A>T	GRCh37
NC_000009.10:g.135121253A>T	NCBI36
NG_006669.1:g.21623T>A
NG_006669.2:g.24171T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.715T>A
ENST00000647353.1:n.54-4893T>A
ENST00000679909.1:c.28+19117T>A	ENSP00000506089.1:n.28+19117T>A
ENST00000453660.3:n.697T>A
ENST00000538324.2:c.683T>A	ENSP00000483018.1:p.Phe228Tyr
ENST00000611156.4:c.683T>A	ENSP00000483265.1:p.Phe228Tyr
NM_020469.2:c.686T>A	NP_065202.2:p.Phe229Tyr
NM_020469.3:c.686T>A	NP_065202.2:p.Phe229Tyr