Canonical Allele Identifier: CA5305910
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs8176720

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257486T>C , CM000671.2:g.133257486T>C GRCh38
NC_000009.11:g.136132873T>C , CM000671.1:g.136132873T>C GRCh37
NC_000009.10:g.135122694T>C NCBI36
NG_006669.1:g.20182A>G
NG_006669.2:g.22730A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.326A>G
ENST00000647353.1:n.54-6334A>G
ENST00000651471.1:n.329+556A>G
ENST00000679909.1:c.28+17676A>G ENSP00000506089.1:n.28+17676A>G
ENST00000453660.3:n.308A>G
ENST00000538324.2:c.294A>G ENSP00000483018.1:p.Thr98=
ENST00000611156.4:c.294A>G ENSP00000483265.1:p.Thr98=
NM_020469.2:c.297A>G NP_065202.2:p.Thr99=
NM_020469.3:c.297A>G NP_065202.2:p.Thr99=