Canonical Allele Identifier: CA1129717046

Gene: ABO

Linked Data

• dbSNP Id: rs1588640833
• gnomAD v3: 9-133260120-A-G
• gnomAD v4: 9-133260120-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260120A>G , CM000671.2:g.133260120A>G	GRCh38
NC_000009.11:g.136135524A>G , CM000671.1:g.136135524A>G	GRCh37
NC_000009.10:g.135125345A>G	NCBI36
NG_006669.1:g.17530T>C
NG_006669.2:g.20095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.186-254T>C
ENST00000647353.1:n.54-8968T>C
ENST00000651471.1:n.191-254T>C
ENST00000679909.1:c.28+15042T>C	ENSP00000506089.1:n.28+15042T>C
ENST00000453660.3:n.168-254T>C
ENST00000538324.2:c.156-254T>C	ENSP00000483018.1:n.156-254T>C
ENST00000611156.4:c.156-254T>C	ENSP00000483265.1:n.156-254T>C
NM_020469.2:c.156-254T>C	NP_065202.2:n.156-254T>C
NM_020469.3:c.156-254T>C	NP_065202.2:n.156-254T>C