Canonical Allele Identifier: CA860754209
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1396014234

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257074del , CM000671.2:g.133257074del GRCh38
NC_000009.11:g.136132461del , CM000671.1:g.136132461del GRCh37
NC_000009.10:g.135122282del NCBI36
NG_006669.1:g.20594del
NG_006669.2:g.23142del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+335del
ENST00000647353.1:n.54-5922del
ENST00000651471.1:n.330-718del
ENST00000679909.1:c.28+18088del ENSP00000506089.1:n.28+18088del
ENST00000453660.3:n.385+335del
ENST00000538324.2:c.371+335del ENSP00000483018.1:n.371+335del
ENST00000611156.4:c.371+335del ENSP00000483265.1:n.371+335del
NM_020469.2:c.374+335del NP_065202.2:n.374+335del
NM_020469.3:c.374+335del NP_065202.2:n.374+335del