ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA375685798
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131476C>G (hg19)
chr9:g.133256089C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256089C>G , CM000671.2:g.133256089C>G
GRCh38
NC_000009.11:g.136131476C>G , CM000671.1:g.136131476C>G
GRCh37
NC_000009.10:g.135121297C>G
NCBI36
NG_006669.1:g.21579G>C
NG_006669.2:g.24127G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.671G>C
ENST00000647353.1:n.54-4937G>C
ENST00000679909.1:c.28+19073G>C
ENSP00000506089.1:n.28+19073G>C
ENST00000453660.3:n.653G>C
ENST00000538324.2:c.639G>C
ENSP00000483018.1:p.Met213Ile
ENST00000611156.4:c.639G>C
ENSP00000483265.1:p.Met213Ile
NM_020469.2:c.642G>C
NP_065202.2:p.Met214Ile
NM_020469.3:c.642G>C
NP_065202.2:p.Met214Ile
Search 100 bp 5'
Search 100 bp 3'