Canonical Allele Identifier: CA375407755
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136501754T>A (hg19) chr9:g.133636632T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636632T>A , CM000671.2:g.133636632T>A GRCh38
NC_000009.11:g.136501754T>A , CM000671.1:g.136501754T>A GRCh37
NC_000009.10:g.135491575T>A NCBI36
NG_008645.1:g.5270T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.255T>A ENSP00000263611.3:p.Phe85Leu
ENST00000393056.8:c.261T>A MANE Select ENSP00000376776.2:p.Phe87Leu
ENST00000263611.2:c.219T>A ENSP00000263611.2:p.Phe73Leu
ENST00000393056.6:c.261T>A ENSP00000376776.2:p.Phe87Leu
NM_000787.3:c.261T>A NP_000778.3:p.Phe87Leu
NM_000787.4:c.261T>A MANE Select NP_000778.3:p.Phe87Leu
Search 100 bp 5'
Search 100 bp 3'