Canonical Allele Identifier: CA375686110

Gene: ABO

Linked Data

• dbSNP Id: rs1333307367
• MyVariant Identifiers: chr9:g.136131552A>T (hg19) ; chr9:g.133256165A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256165A>T , CM000671.2:g.133256165A>T	GRCh38
NC_000009.11:g.136131552A>T , CM000671.1:g.136131552A>T	GRCh37
NC_000009.10:g.135121373A>T	NCBI36
NG_006669.1:g.21503T>A
NG_006669.2:g.24051T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.595T>A
ENST00000647353.1:n.54-5013T>A
ENST00000651471.1:n.521T>A
ENST00000679909.1:c.28+18997T>A	ENSP00000506089.1:n.28+18997T>A
ENST00000453660.3:n.577T>A
ENST00000538324.2:c.563T>A	ENSP00000483018.1:p.Met188Lys
ENST00000611156.4:c.563T>A	ENSP00000483265.1:p.Met188Lys
NM_020469.2:c.566T>A	NP_065202.2:p.Met189Lys
NM_020469.3:c.566T>A	NP_065202.2:p.Met189Lys