Canonical Allele Identifier: CA5313244
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs371162663
ExAC: 9:136509313 G / A
gnomAD v2: 9-136509313-G-A
gnomAD v3: 9-133644191-G-A
gnomAD v4: 9-133644191-G-A
MyVariant Identifiers: chr9:g.136509313G>A (hg19) chr9:g.133644191G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644191G>A , CM000671.2:g.133644191G>A GRCh38
NC_000009.11:g.136509313G>A , CM000671.1:g.136509313G>A GRCh37
NC_000009.10:g.135499134G>A NCBI36
NG_008645.1:g.12829G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-27G>A MANE Select ENSP00000376776.2:n.922-27G>A
ENST00000393056.6:c.922-27G>A ENSP00000376776.2:n.922-27G>A
NM_000787.3:c.922-27G>A NP_000778.3:n.922-27G>A
NM_000787.4:c.922-27G>A MANE Select NP_000778.3:n.922-27G>A
Search 100 bp 5'
Search 100 bp 3'