Canonical Allele Identifier: CA375686119

Gene: ABO

Linked Data

• gnomAD v4: 9-133256171-C-A
• MyVariant Identifiers: chr9:g.136131558C>A (hg19) ; chr9:g.133256171C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256171C>A , CM000671.2:g.133256171C>A	GRCh38
NC_000009.11:g.136131558C>A , CM000671.1:g.136131558C>A	GRCh37
NC_000009.10:g.135121379C>A	NCBI36
NG_006669.1:g.21497G>T
NG_006669.2:g.24045G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.589G>T
ENST00000647353.1:n.54-5019G>T
ENST00000651471.1:n.515G>T
ENST00000679909.1:c.28+18991G>T	ENSP00000506089.1:n.28+18991G>T
ENST00000453660.3:n.571G>T
ENST00000538324.2:c.557G>T	ENSP00000483018.1:p.Arg186Leu
ENST00000611156.4:c.557G>T	ENSP00000483265.1:p.Arg186Leu
NM_020469.2:c.560G>T	NP_065202.2:p.Arg187Leu
NM_020469.3:c.560G>T	NP_065202.2:p.Arg187Leu