Canonical Allele Identifier: CA2692330596
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133257603-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257603T>G , CM000671.2:g.133257603T>G GRCh38
NC_000009.11:g.136132990T>G , CM000671.1:g.136132990T>G GRCh37
NC_000009.10:g.135122811T>G NCBI36
NG_006669.1:g.20064A>C
NG_006669.2:g.22612A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-61A>C
ENST00000647353.1:n.54-6451A>C
ENST00000651471.1:n.329+439A>C
ENST00000679909.1:c.28+17559A>C ENSP00000506089.1:n.28+17559A>C
ENST00000453660.3:n.252-61A>C
ENST00000538324.2:c.240-61A>C ENSP00000483018.1:n.240-61A>C
ENST00000611156.4:c.240-61A>C ENSP00000483265.1:n.240-61A>C
NM_020469.2:c.240-61A>C NP_065202.2:n.240-61A>C
NM_020469.3:c.240-61A>C NP_065202.2:n.240-61A>C
Search 100 bp 5'
Search 100 bp 3'