Canonical Allele Identifier: CA860776555
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1404842420
gnomAD v4: 9-133644102-G-A
MyVariant Identifiers: chr9:g.136509224G>A (hg19) chr9:g.133644102G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644102G>A , CM000671.2:g.133644102G>A GRCh38
NC_000009.11:g.136509224G>A , CM000671.1:g.136509224G>A GRCh37
NC_000009.10:g.135499045G>A NCBI36
NG_008645.1:g.12740G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-116G>A MANE Select ENSP00000376776.2:n.922-116G>A
ENST00000393056.6:c.922-116G>A ENSP00000376776.2:n.922-116G>A
NM_000787.3:c.922-116G>A NP_000778.3:n.922-116G>A
NM_000787.4:c.922-116G>A MANE Select NP_000778.3:n.922-116G>A
Search 100 bp 5'
Search 100 bp 3'