Canonical Allele Identifier: CA2692330780
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258033del , CM000671.2:g.133258033del GRCh38
NC_000009.11:g.136133423del , CM000671.1:g.136133423del GRCh37
NC_000009.10:g.135123244del NCBI36
NG_006669.1:g.19633del
NG_006669.2:g.22184del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+66del
ENST00000647353.1:n.54-6879del
ENST00000651471.1:n.329+11del
ENST00000679909.1:c.28+17131del ENSP00000506089.1:n.28+17131del
ENST00000453660.3:n.251+66del
ENST00000538324.2:c.239+66del ENSP00000483018.1:n.239+66del
ENST00000611156.4:c.239+66del ENSP00000483265.1:n.239+66del
NM_020469.2:c.239+66del NP_065202.2:n.239+66del
NM_020469.3:c.239+66del NP_065202.2:n.239+66del