Canonical Allele Identifier: CA5305769

Gene: ABO

Linked Data

• dbSNP Id: rs781897939
• ExAC: 9:136131438 G / A
• gnomAD v2: 9-136131438-G-A
• gnomAD v4: 9-133256051-G-A
• MyVariant Identifiers: chr9:g.136131438G>A (hg19) ; chr9:g.133256051G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256051G>A , CM000671.2:g.133256051G>A	GRCh38
NC_000009.11:g.136131438G>A , CM000671.1:g.136131438G>A	GRCh37
NC_000009.10:g.135121259G>A	NCBI36
NG_006669.1:g.21617C>T
NG_006669.2:g.24165C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.709C>T
ENST00000647353.1:n.54-4899C>T
ENST00000679909.1:c.28+19111C>T	ENSP00000506089.1:n.28+19111C>T
ENST00000453660.3:n.691C>T
ENST00000538324.2:c.677C>T	ENSP00000483018.1:p.Pro226Leu
ENST00000611156.4:c.677C>T	ENSP00000483265.1:p.Pro226Leu
NM_020469.2:c.680C>T	NP_065202.2:p.Pro227Leu
NM_020469.3:c.680C>T	NP_065202.2:p.Pro227Leu