Canonical Allele Identifier: CA375686324
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256276A>C , CM000671.2:g.133256276A>C GRCh38
NC_000009.11:g.136131663A>C , CM000671.1:g.136131663A>C GRCh37
NC_000009.10:g.135121484A>C NCBI36
NG_006669.1:g.21392T>G
NG_006669.2:g.23940T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.484T>G
ENST00000647353.1:n.54-5124T>G
ENST00000651471.1:n.410T>G
ENST00000679909.1:c.28+18886T>G ENSP00000506089.1:n.28+18886T>G
ENST00000453660.3:n.466T>G
ENST00000538324.2:c.452T>G ENSP00000483018.1:p.Phe151Cys
ENST00000611156.4:c.452T>G ENSP00000483265.1:p.Phe151Cys
NM_020469.2:c.455T>G NP_065202.2:p.Phe152Cys
NM_020469.3:c.455T>G NP_065202.2:p.Phe152Cys