Canonical Allele Identifier: CA860756257

Gene: ABO

Linked Data

• dbSNP Id: rs1301844628
• MyVariant Identifiers: chr9:g.133260375G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260375G>A , CM000671.2:g.133260375G>A	GRCh38
NC_000009.11:g.136135778G>A , CM000671.1:g.136135778G>A	GRCh37
NC_000009.10:g.135125599G>A	NCBI36
NG_006669.1:g.17275C>T
NG_006669.2:g.19840C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.186-509C>T
ENST00000647353.1:n.54-9223C>T
ENST00000651471.1:n.191-509C>T
ENST00000679909.1:c.28+14787C>T	ENSP00000506089.1:n.28+14787C>T
ENST00000453660.3:n.168-509C>T
ENST00000538324.2:c.156-509C>T	ENSP00000483018.1:n.156-509C>T
ENST00000611156.4:c.156-509C>T	ENSP00000483265.1:n.156-509C>T
NM_020469.2:c.156-509C>T	NP_065202.2:n.156-509C>T
NM_020469.3:c.156-509C>T	NP_065202.2:n.156-509C>T