Canonical Allele Identifier: CA467779985

Gene: ABO

Linked Data

• gnomAD v3: 9-133255303-A-G
• gnomAD v4: 9-133255303-A-G
• MyVariant Identifiers: chr9:g.136130690A>G (hg19)

Genomic Alleles

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

Transcript Alleles

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