Canonical Allele Identifier: CA467613783
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509357G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644235G>A , CM000671.2:g.133644235G>A GRCh38
NC_000009.11:g.136509357G>A , CM000671.1:g.136509357G>A GRCh37
NC_000009.10:g.135499178G>A NCBI36
NG_008645.1:g.12873G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.939G>A MANE Select ENSP00000376776.2:p.Glu313=
ENST00000393056.6:c.939G>A ENSP00000376776.2:p.Glu313=
NM_000787.3:c.939G>A NP_000778.3:p.Glu313=
NM_000787.4:c.939G>A MANE Select NP_000778.3:p.Glu313=
Search 100 bp 5'
Search 100 bp 3'