Canonical Allele Identifier: CA2692392595
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133636719-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636719C>A , CM000671.2:g.133636719C>A GRCh38
NC_000009.11:g.136501841C>A , CM000671.1:g.136501841C>A GRCh37
NC_000009.10:g.135491662C>A NCBI36
NG_008645.1:g.5357C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+9C>A ENSP00000263611.3:n.333+9C>A
ENST00000393056.8:c.339+9C>A MANE Select ENSP00000376776.2:n.339+9C>A
ENST00000263611.2:c.297+9C>A ENSP00000263611.2:n.297+9C>A
ENST00000393056.6:c.339+9C>A ENSP00000376776.2:n.339+9C>A
NM_000787.3:c.339+9C>A NP_000778.3:n.339+9C>A
NM_000787.4:c.339+9C>A MANE Select NP_000778.3:n.339+9C>A
Search 100 bp 5'
Search 100 bp 3'