Canonical Allele Identifier: CA467782902

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131626C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256239C>T , CM000671.2:g.133256239C>T	GRCh38
NC_000009.11:g.136131626C>T , CM000671.1:g.136131626C>T	GRCh37
NC_000009.10:g.135121447C>T	NCBI36
NG_006669.1:g.21429G>A
NG_006669.2:g.23977G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.521G>A
ENST00000647353.1:n.54-5087G>A
ENST00000651471.1:n.447G>A
ENST00000679909.1:c.28+18923G>A	ENSP00000506089.1:n.28+18923G>A
ENST00000453660.3:n.503G>A
ENST00000538324.2:c.489G>A	ENSP00000483018.1:p.Leu163=
ENST00000611156.4:c.489G>A	ENSP00000483265.1:p.Leu163=
NM_020469.2:c.492G>A	NP_065202.2:p.Leu164=
NM_020469.3:c.492G>A	NP_065202.2:p.Leu164=