Canonical Allele Identifier: CA200951877
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs368831459
gnomAD v4: 9-133636631-T-A
MyVariant Identifiers: chr9:g.136501753T>A (hg19) chr9:g.133636631T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636631T>A , CM000671.2:g.133636631T>A GRCh38
NC_000009.11:g.136501753T>A , CM000671.1:g.136501753T>A GRCh37
NC_000009.10:g.135491574T>A NCBI36
NG_008645.1:g.5269T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.254T>A ENSP00000263611.3:p.Phe85Tyr
ENST00000393056.8:c.260T>A MANE Select ENSP00000376776.2:p.Phe87Tyr
ENST00000263611.2:c.218T>A ENSP00000263611.2:p.Phe73Tyr
ENST00000393056.6:c.260T>A ENSP00000376776.2:p.Phe87Tyr
NM_000787.3:c.260T>A NP_000778.3:p.Phe87Tyr
NM_000787.4:c.260T>A MANE Select NP_000778.3:p.Phe87Tyr
Search 100 bp 5'
Search 100 bp 3'