Canonical Allele Identifier: CA200765911
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs8176729

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257141A>C , CM000671.2:g.133257141A>C GRCh38
NC_000009.11:g.136132528A>C , CM000671.1:g.136132528A>C GRCh37
NC_000009.10:g.135122349A>C NCBI36
NG_006669.1:g.20527T>G
NG_006669.2:g.23075T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+268T>G
ENST00000647353.1:n.54-5989T>G
ENST00000651471.1:n.330-785T>G
ENST00000679909.1:c.28+18021T>G ENSP00000506089.1:n.28+18021T>G
ENST00000453660.3:n.385+268T>G
ENST00000538324.2:c.371+268T>G ENSP00000483018.1:n.371+268T>G
ENST00000611156.4:c.371+268T>G ENSP00000483265.1:n.371+268T>G
NM_020469.2:c.374+268T>G NP_065202.2:n.374+268T>G
NM_020469.3:c.374+268T>G NP_065202.2:n.374+268T>G