Canonical Allele Identifier: CA1129756818
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1832080823
gnomAD v3: 9-133638725-A-G
gnomAD v4: 9-133638725-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638725A>G , CM000671.2:g.133638725A>G GRCh38
NC_000009.11:g.136503847A>G , CM000671.1:g.136503847A>G GRCh37
NC_000009.10:g.135493668A>G NCBI36
NG_008645.1:g.7363A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+2015A>G ENSP00000263611.3:n.333+2015A>G
ENST00000393056.8:c.340-1121A>G MANE Select ENSP00000376776.2:n.340-1121A>G
ENST00000263611.2:c.297+2015A>G ENSP00000263611.2:n.297+2015A>G
ENST00000393056.6:c.340-1121A>G ENSP00000376776.2:n.340-1121A>G
NM_000787.3:c.340-1121A>G NP_000778.3:n.340-1121A>G
NM_000787.4:c.340-1121A>G MANE Select NP_000778.3:n.340-1121A>G
Search 100 bp 5'
Search 100 bp 3'