Canonical Allele Identifier: CA860755396

Gene: ABO

Linked Data

• dbSNP Id: rs1371610311
• MyVariant Identifiers: chr9:g.136133782G>A (hg19) ; chr9:g.133258391G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258391G>A , CM000671.2:g.133258391G>A	GRCh38
NC_000009.11:g.136133782G>A , CM000671.1:g.136133782G>A	GRCh37
NC_000009.10:g.135123603G>A	NCBI36
NG_006669.1:g.19272C>T
NG_006669.2:g.21824C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-259C>T
ENST00000647353.1:n.54-7239C>T
ENST00000651471.1:n.239-259C>T
ENST00000679909.1:c.28+16771C>T	ENSP00000506089.1:n.28+16771C>T
ENST00000453660.3:n.216-259C>T
ENST00000538324.2:c.204-259C>T	ENSP00000483018.1:n.204-259C>T
ENST00000611156.4:c.204-259C>T	ENSP00000483265.1:n.204-259C>T
NM_020469.2:c.204-259C>T	NP_065202.2:n.204-259C>T
NM_020469.3:c.204-259C>T	NP_065202.2:n.204-259C>T