Canonical Allele Identifier: CA467853027

Gene: ABO

Linked Data

• dbSNP Id: rs2118942460
• MyVariant Identifiers: chr9:g.136131497C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256110C>T , CM000671.2:g.133256110C>T	GRCh38
NC_000009.11:g.136131497C>T , CM000671.1:g.136131497C>T	GRCh37
NC_000009.10:g.135121318C>T	NCBI36
NG_006669.1:g.21558G>A
NG_006669.2:g.24106G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.650G>A
ENST00000647353.1:n.54-4958G>A
ENST00000651471.1:n.576G>A
ENST00000679909.1:c.28+19052G>A	ENSP00000506089.1:n.28+19052G>A
ENST00000453660.3:n.632G>A
ENST00000538324.2:c.618G>A	ENSP00000483018.1:p.Leu206=
ENST00000611156.4:c.618G>A	ENSP00000483265.1:p.Leu206=
NM_020469.2:c.621G>A	NP_065202.2:p.Leu207=
NM_020469.3:c.621G>A	NP_065202.2:p.Leu207=