Canonical Allele Identifier: CA1882580970
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256331G= , CM000671.2:g.133256331G= GRCh38
NC_000009.11:g.136131718G= , CM000671.1:g.136131718G= GRCh37
NC_000009.10:g.135121539G= NCBI36
NG_006669.1:g.21337C=
NG_006669.2:g.23885C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.429C=
ENST00000647353.1:n.54-5179C=
ENST00000651471.1:n.355C=
ENST00000679909.1:c.28+18831C= ENSP00000506089.1:n.28+18831C=
ENST00000453660.3:n.411C=
ENST00000538324.2:c.397C= ENSP00000483018.1:p.Leu133=
ENST00000611156.4:c.397C= ENSP00000483265.1:p.Leu133=
NM_020469.2:c.400C= NP_065202.2:p.Leu134=
NM_020469.3:c.400C= NP_065202.2:p.Leu134=