Canonical Allele Identifier: CA375686343
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256284G>C , CM000671.2:g.133256284G>C GRCh38
NC_000009.11:g.136131671G>C , CM000671.1:g.136131671G>C GRCh37
NC_000009.10:g.135121492G>C NCBI36
NG_006669.1:g.21384C>G
NG_006669.2:g.23932C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.476C>G
ENST00000647353.1:n.54-5132C>G
ENST00000651471.1:n.402C>G
ENST00000679909.1:c.28+18878C>G ENSP00000506089.1:n.28+18878C>G
ENST00000453660.3:n.458C>G
ENST00000538324.2:c.444C>G ENSP00000483018.1:p.Tyr148Ter
ENST00000611156.4:c.444C>G ENSP00000483265.1:p.Tyr148Ter
NM_020469.2:c.447C>G NP_065202.2:p.Tyr149Ter
NM_020469.3:c.447C>G NP_065202.2:p.Tyr149Ter