Canonical Allele Identifier: CA200951865
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs917323889
gnomAD v4: 9-133636629-G-C
MyVariant Identifiers: chr9:g.136501751G>C (hg19) chr9:g.133636629G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.252G>C ENSP00000263611.3:p.Leu84=
ENST00000393056.8:c.258G>C MANE Select ENSP00000376776.2:p.Leu86=
ENST00000263611.2:c.216G>C ENSP00000263611.2:p.Leu72=
ENST00000393056.6:c.258G>C ENSP00000376776.2:p.Leu86=
NM_000787.3:c.258G>C NP_000778.3:p.Leu86=
NM_000787.4:c.258G>C MANE Select NP_000778.3:p.Leu86=
Search 100 bp 5'
Search 100 bp 3'