Canonical Allele Identifier: CA200765877

Gene: ABO

Linked Data

• dbSNP Id: rs1009011562
• MyVariant Identifiers: chr9:g.136132454C>A (hg19) ; chr9:g.133257067C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257067C>A , CM000671.2:g.133257067C>A	GRCh38
NC_000009.11:g.136132454C>A , CM000671.1:g.136132454C>A	GRCh37
NC_000009.10:g.135122275C>A	NCBI36
NG_006669.1:g.20601G>T
NG_006669.2:g.23149G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.403+342G>T
ENST00000647353.1:n.54-5915G>T
ENST00000651471.1:n.330-711G>T
ENST00000679909.1:c.28+18095G>T	ENSP00000506089.1:n.28+18095G>T
ENST00000453660.3:n.385+342G>T
ENST00000538324.2:c.371+342G>T	ENSP00000483018.1:n.371+342G>T
ENST00000611156.4:c.371+342G>T	ENSP00000483265.1:n.371+342G>T
NM_020469.2:c.374+342G>T	NP_065202.2:n.374+342G>T
NM_020469.3:c.374+342G>T	NP_065202.2:n.374+342G>T