ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA375682231
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131020G>A (hg19)
chr9:g.133255633G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255633G>A , CM000671.2:g.133255633G>A
GRCh38
NC_000009.11:g.136131020G>A , CM000671.1:g.136131020G>A
GRCh37
NC_000009.10:g.135120841G>A
NCBI36
NG_006669.1:g.22035C>T
NG_006669.2:g.24583C>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.1127C>T
ENST00000647353.1:n.54-4481C>T
ENST00000679909.1:c.28+19529C>T
ENSP00000506089.1:n.28+19529C>T
ENST00000453660.3:n.1109C>T
ENST00000538324.2:c.1091C>T
ENSP00000483018.1:p.Ala364Val
ENST00000611156.4:c.*33C>T
ENSP00000483265.1:n.*33C>T
NM_020469.2:c.*33C>T
NP_065202.2:n.*33C>T
NM_020469.3:c.*33C>T
NP_065202.2:n.*33C>T
Search 100 bp 5'
Search 100 bp 3'