Canonical Allele Identifier: CA1882581922
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256970G= , CM000671.2:g.133256970G= GRCh38
NC_000009.11:g.136132357G= , CM000671.1:g.136132357G= GRCh37
NC_000009.10:g.135122178G= NCBI36
NG_006669.1:g.20698C=
NG_006669.2:g.23246C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+439C=
ENST00000647353.1:n.54-5818C=
ENST00000651471.1:n.330-614C=
ENST00000679909.1:c.28+18192C= ENSP00000506089.1:n.28+18192C=
ENST00000453660.3:n.385+439C=
ENST00000538324.2:c.371+439C= ENSP00000483018.1:n.371+439C=
ENST00000611156.4:c.371+439C= ENSP00000483265.1:n.371+439C=
NM_020469.2:c.374+439C= NP_065202.2:n.374+439C=
NM_020469.3:c.374+439C= NP_065202.2:n.374+439C=