Canonical Allele Identifier: CA375407747
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136501752T>A (hg19) chr9:g.133636630T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636630T>A , CM000671.2:g.133636630T>A GRCh38
NC_000009.11:g.136501752T>A , CM000671.1:g.136501752T>A GRCh37
NC_000009.10:g.135491573T>A NCBI36
NG_008645.1:g.5268T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.253T>A ENSP00000263611.3:p.Phe85Ile
ENST00000393056.8:c.259T>A MANE Select ENSP00000376776.2:p.Phe87Ile
ENST00000263611.2:c.217T>A ENSP00000263611.2:p.Phe73Ile
ENST00000393056.6:c.259T>A ENSP00000376776.2:p.Phe87Ile
NM_000787.3:c.259T>A NP_000778.3:p.Phe87Ile
NM_000787.4:c.259T>A MANE Select NP_000778.3:p.Phe87Ile
Search 100 bp 5'
Search 100 bp 3'