Canonical Allele Identifier: CA1882581919
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256963T= , CM000671.2:g.133256963T= GRCh38
NC_000009.11:g.136132350T= , CM000671.1:g.136132350T= GRCh37
NC_000009.10:g.135122171T= NCBI36
NG_006669.1:g.20705A=
NG_006669.2:g.23253A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+446A=
ENST00000647353.1:n.54-5811A=
ENST00000651471.1:n.330-607A=
ENST00000679909.1:c.28+18199A= ENSP00000506089.1:n.28+18199A=
ENST00000453660.3:n.385+446A=
ENST00000538324.2:c.371+446A= ENSP00000483018.1:n.371+446A=
ENST00000611156.4:c.371+446A= ENSP00000483265.1:n.371+446A=
NM_020469.2:c.374+446A= NP_065202.2:n.374+446A=
NM_020469.3:c.374+446A= NP_065202.2:n.374+446A=