Canonical Allele Identifier: CA2580907972
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257138T>G , CM000671.2:g.133257138T>G GRCh38
NC_000009.11:g.136132525T>G , CM000671.1:g.136132525T>G GRCh37
NC_000009.10:g.135122346T>G NCBI36
NG_006669.1:g.20530A>C
NG_006669.2:g.23078A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+271A>C
ENST00000647353.1:n.54-5986A>C
ENST00000651471.1:n.330-782A>C
ENST00000679909.1:c.28+18024A>C ENSP00000506089.1:n.28+18024A>C
ENST00000453660.3:n.385+271A>C
ENST00000538324.2:c.371+271A>C ENSP00000483018.1:n.371+271A>C
ENST00000611156.4:c.371+271A>C ENSP00000483265.1:n.371+271A>C
NM_020469.2:c.374+271A>C NP_065202.2:n.374+271A>C
NM_020469.3:c.374+271A>C NP_065202.2:n.374+271A>C