Canonical Allele Identifier: CA467780797
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130832T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255445T>C , CM000671.2:g.133255445T>C GRCh38
NC_000009.11:g.136130832T>C , CM000671.1:g.136130832T>C GRCh37
NC_000009.10:g.135120653T>C NCBI36
NG_006669.1:g.22223A>G
NG_006669.2:g.24771A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1315A>G
ENST00000647353.1:n.54-4293A>G
ENST00000679909.1:c.28+19717A>G ENSP00000506089.1:n.28+19717A>G
ENST00000453660.3:n.1297A>G
ENST00000611156.4:c.*221A>G ENSP00000483265.1:n.*221A>G
NM_020469.2:c.*221A>G NP_065202.2:n.*221A>G
NM_020469.3:c.*221A>G NP_065202.2:n.*221A>G