Canonical Allele Identifier: CA200764951

Gene: ABO

Linked Data

• dbSNP Id: rs5901010
• MyVariant Identifiers: chr9:g.136130849G>C (hg19) ; chr9:g.133255462G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255462G>C , CM000671.2:g.133255462G>C	GRCh38
NC_000009.11:g.136130849G>C , CM000671.1:g.136130849G>C	GRCh37
NC_000009.10:g.135120670G>C	NCBI36
NG_006669.1:g.22206C>G
NG_006669.2:g.24754C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1298C>G
ENST00000647353.1:n.54-4310C>G
ENST00000679909.1:c.28+19700C>G	ENSP00000506089.1:n.28+19700C>G
ENST00000453660.3:n.1280C>G
ENST00000611156.4:c.*204C>G	ENSP00000483265.1:n.*204C>G
NM_020469.2:c.*204C>G	NP_065202.2:n.*204C>G
NM_020469.3:c.*204C>G	NP_065202.2:n.*204C>G