Canonical Allele Identifier: CA860772800
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1396065435
MyVariant Identifiers: chr9:g.136503845G>A (hg19) chr9:g.133638723G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638723G>A , CM000671.2:g.133638723G>A GRCh38
NC_000009.11:g.136503845G>A , CM000671.1:g.136503845G>A GRCh37
NC_000009.10:g.135493666G>A NCBI36
NG_008645.1:g.7361G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+2013G>A ENSP00000263611.3:n.333+2013G>A
ENST00000393056.8:c.340-1123G>A MANE Select ENSP00000376776.2:n.340-1123G>A
ENST00000263611.2:c.297+2013G>A ENSP00000263611.2:n.297+2013G>A
ENST00000393056.6:c.340-1123G>A ENSP00000376776.2:n.340-1123G>A
NM_000787.3:c.340-1123G>A NP_000778.3:n.340-1123G>A
NM_000787.4:c.340-1123G>A MANE Select NP_000778.3:n.340-1123G>A
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