Canonical Allele Identifier: CA200957426
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs973820464
gnomAD v3: 9-133638696-GT-G
gnomAD v4: 9-133638696-GT-G
MyVariant Identifiers: chr9:g.136503819del (hg19) chr9:g.133638697del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638697del , CM000671.2:g.133638697del GRCh38
NC_000009.11:g.136503819del , CM000671.1:g.136503819del GRCh37
NC_000009.10:g.135493640del NCBI36
NG_008645.1:g.7335del

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+1987del ENSP00000263611.3:n.333+1987del
ENST00000393056.8:c.340-1149del MANE Select ENSP00000376776.2:n.340-1149del
ENST00000263611.2:c.297+1987del ENSP00000263611.2:n.297+1987del
ENST00000393056.6:c.340-1149del ENSP00000376776.2:n.340-1149del
NM_000787.3:c.340-1149del NP_000778.3:n.340-1149del
NM_000787.4:c.340-1149del MANE Select NP_000778.3:n.340-1149del
Search 100 bp 5'
Search 100 bp 3'