Canonical Allele Identifier: CA591309068
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1281842203

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257645C>T , CM000671.2:g.133257645C>T GRCh38
NC_000009.11:g.136133032C>T , CM000671.1:g.136133032C>T GRCh37
NC_000009.10:g.135122853C>T NCBI36
NG_006669.1:g.20022G>A
NG_006669.2:g.22570G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-103G>A
ENST00000647353.1:n.54-6493G>A
ENST00000651471.1:n.329+397G>A
ENST00000679909.1:c.28+17517G>A ENSP00000506089.1:n.28+17517G>A
ENST00000453660.3:n.252-103G>A
ENST00000538324.2:c.240-103G>A ENSP00000483018.1:n.240-103G>A
ENST00000611156.4:c.240-103G>A ENSP00000483265.1:n.240-103G>A
NM_020469.2:c.240-103G>A NP_065202.2:n.240-103G>A
NM_020469.3:c.240-103G>A NP_065202.2:n.240-103G>A