Canonical Allele Identifier: CA860757199

Gene: ABO

Linked Data

• dbSNP Id: rs1318061623
• gnomAD v3: 9-133261660-T-C
• gnomAD v4: 9-133261660-T-C
• MyVariant Identifiers: chr9:g.133261660T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261660T>C , CM000671.2:g.133261660T>C	GRCh38
NC_000009.11:g.136137063T>C , CM000671.1:g.136137063T>C	GRCh37
NC_000009.10:g.135126884T>C	NCBI36
NG_006669.1:g.15990A>G
NG_006669.2:g.18555A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.129-286A>G
ENST00000647353.1:n.54-10508A>G
ENST00000651471.1:n.134-286A>G
ENST00000679909.1:c.28+13502A>G	ENSP00000506089.1:n.28+13502A>G
ENST00000453660.3:n.111-286A>G
ENST00000538324.2:c.99-286A>G	ENSP00000483018.1:n.99-286A>G
ENST00000611156.4:c.99-286A>G	ENSP00000483265.1:n.99-286A>G
NM_020469.2:c.99-286A>G	NP_065202.2:n.99-286A>G
NM_020469.3:c.99-286A>G	NP_065202.2:n.99-286A>G