Canonical Allele Identifier: CA2692330582
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257583G>T , CM000671.2:g.133257583G>T GRCh38
NC_000009.11:g.136132970G>T , CM000671.1:g.136132970G>T GRCh37
NC_000009.10:g.135122791G>T NCBI36
NG_006669.1:g.20084C>A
NG_006669.2:g.22632C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-41C>A
ENST00000647353.1:n.54-6431C>A
ENST00000651471.1:n.329+459C>A
ENST00000679909.1:c.28+17579C>A ENSP00000506089.1:n.28+17579C>A
ENST00000453660.3:n.252-41C>A
ENST00000538324.2:c.240-41C>A ENSP00000483018.1:n.240-41C>A
ENST00000611156.4:c.240-41C>A ENSP00000483265.1:n.240-41C>A
NM_020469.2:c.240-41C>A NP_065202.2:n.240-41C>A
NM_020469.3:c.240-41C>A NP_065202.2:n.240-41C>A