Canonical Allele Identifier: CA1882582043
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834609659

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257118G>C , CM000671.2:g.133257118G>C GRCh38
NC_000009.11:g.136132505G>C , CM000671.1:g.136132505G>C GRCh37
NC_000009.10:g.135122326G>C NCBI36
NG_006669.1:g.20550C>G
NG_006669.2:g.23098C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+291C>G
ENST00000647353.1:n.54-5966C>G
ENST00000651471.1:n.330-762C>G
ENST00000679909.1:c.28+18044C>G ENSP00000506089.1:n.28+18044C>G
ENST00000453660.3:n.385+291C>G
ENST00000538324.2:c.371+291C>G ENSP00000483018.1:n.371+291C>G
ENST00000611156.4:c.371+291C>G ENSP00000483265.1:n.371+291C>G
NM_020469.2:c.374+291C>G NP_065202.2:n.374+291C>G
NM_020469.3:c.374+291C>G NP_065202.2:n.374+291C>G