×
SERVICES INTERRUPTION:
2026-08-07T10:00:00-0500
—
2026-08-14T18:00:00-0500
Allele Registry, ERepo, and Actionability UI services may experience intermittent service interruptions during this period.
ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA1882777332
Community Standard Title: NM_000787.4(DBH):c.1024+192T=
Gene: DBH
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133644512T= , CM000671.2:g.133644512T=
GRCh38
NC_000009.11:g.136509634T= , CM000671.1:g.136509634T=
GRCh37
NC_000009.10:g.135499455T=
NCBI36
NG_008645.1:g.13150T=
Transcript Alleles
HGVS
Amino-acid Change
NM_000787.4:c.1024+192T=
MANE Select
NP_000778.3:n.1024+192T=
ENST00000393056.8:c.1024+192T=
MANE Select
ENSP00000376776.2:n.1024+192T=
NM_000787.3:c.1024+192T=
NP_000778.3:n.1024+192T=
ENST00000393056.6:c.1024+192T=
ENSP00000376776.2:n.1024+192T=
Search 100 bp 5'
Search 100 bp 3'