Canonical Allele Identifier: CA860756126

Gene: ABO

Linked Data

• dbSNP Id: rs1287459599
• gnomAD v3: 9-133260053-T-G
• gnomAD v4: 9-133260053-T-G
• MyVariant Identifiers: chr9:g.133260053T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260053T>G , CM000671.2:g.133260053T>G	GRCh38
NC_000009.11:g.136135457T>G , CM000671.1:g.136135457T>G	GRCh37
NC_000009.10:g.135125278T>G	NCBI36
NG_006669.1:g.17597A>C
NG_006669.2:g.20162A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.186-187A>C
ENST00000647353.1:n.54-8901A>C
ENST00000651471.1:n.191-187A>C
ENST00000679909.1:c.28+15109A>C	ENSP00000506089.1:n.28+15109A>C
ENST00000453660.3:n.168-187A>C
ENST00000538324.2:c.156-187A>C	ENSP00000483018.1:n.156-187A>C
ENST00000611156.4:c.156-187A>C	ENSP00000483265.1:n.156-187A>C
NM_020469.2:c.156-187A>C	NP_065202.2:n.156-187A>C
NM_020469.3:c.156-187A>C	NP_065202.2:n.156-187A>C