Canonical Allele Identifier: CA1129717086
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834685014

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260316G>A , CM000671.2:g.133260316G>A GRCh38
NC_000009.11:g.136135719G>A , CM000671.1:g.136135719G>A GRCh37
NC_000009.10:g.135125540G>A NCBI36
NG_006669.1:g.17334C>T
NG_006669.2:g.19899C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-450C>T
ENST00000647353.1:n.54-9164C>T
ENST00000651471.1:n.191-450C>T
ENST00000679909.1:c.28+14846C>T ENSP00000506089.1:n.28+14846C>T
ENST00000453660.3:n.168-450C>T
ENST00000538324.2:c.156-450C>T ENSP00000483018.1:n.156-450C>T
ENST00000611156.4:c.156-450C>T ENSP00000483265.1:n.156-450C>T
NM_020469.2:c.156-450C>T NP_065202.2:n.156-450C>T
NM_020469.3:c.156-450C>T NP_065202.2:n.156-450C>T