Canonical Allele Identifier: CA467611792
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136501751G>T (hg19)

Genomic Alleles

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

Transcript Alleles

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