Canonical Allele Identifier: CA467611789
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs917323889

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636629G>A , CM000671.2:g.133636629G>A GRCh38
NC_000009.11:g.136501751G>A , CM000671.1:g.136501751G>A GRCh37
NC_000009.10:g.135491572G>A NCBI36
NG_008645.1:g.5267G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.252G>A ENSP00000263611.3:p.Leu84=
ENST00000393056.8:c.258G>A MANE Select ENSP00000376776.2:p.Leu86=
ENST00000263611.2:c.216G>A ENSP00000263611.2:p.Leu72=
ENST00000393056.6:c.258G>A ENSP00000376776.2:p.Leu86=
NM_000787.3:c.258G>A NP_000778.3:p.Leu86=
NM_000787.4:c.258G>A MANE Select NP_000778.3:p.Leu86=