ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA375684359
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131218C>G (hg19)
chr9:g.133255831C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255831C>G , CM000671.2:g.133255831C>G
GRCh38
NC_000009.11:g.136131218C>G , CM000671.1:g.136131218C>G
GRCh37
NC_000009.10:g.135121039C>G
NCBI36
NG_006669.1:g.21837G>C
NG_006669.2:g.24385G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.929G>C
ENST00000647353.1:n.54-4679G>C
ENST00000679909.1:c.28+19331G>C
ENSP00000506089.1:n.28+19331G>C
ENST00000453660.3:n.911G>C
ENST00000538324.2:c.897G>C
ENSP00000483018.1:p.Trp299Cys
ENST00000611156.4:c.897G>C
ENSP00000483265.1:p.Trp299Cys
NM_020469.2:c.900G>C
NP_065202.2:p.Trp300Cys
NM_020469.3:c.900G>C
NP_065202.2:p.Trp300Cys
Search 100 bp 5'
Search 100 bp 3'