Canonical Allele Identifier: CA467779984

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130690A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255303A>C , CM000671.2:g.133255303A>C	GRCh38
NC_000009.11:g.136130690A>C , CM000671.1:g.136130690A>C	GRCh37
NC_000009.10:g.135120511A>C	NCBI36
NG_006669.1:g.22365T>G
NG_006669.2:g.24913T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1457T>G
ENST00000647353.1:n.54-4151T>G
ENST00000679909.1:c.28+19859T>G	ENSP00000506089.1:n.28+19859T>G
ENST00000453660.3:n.1439T>G
ENST00000611156.4:c.*363T>G	ENSP00000483265.1:n.*363T>G
NM_020469.2:c.*363T>G	NP_065202.2:n.*363T>G
NM_020469.3:c.*363T>G	NP_065202.2:n.*363T>G