Canonical Allele Identifier: CA591066593
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1190743749
gnomAD v2: 9-136501860-CAAA-C
gnomAD v3: 9-133636738-CAAA-C
gnomAD v4: 9-133636738-CAAA-C
MyVariant Identifiers: chr9:g.136501861_136501863del (hg19) chr9:g.133636739_133636741del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636739_133636741del , CM000671.2:g.133636739_133636741del GRCh38
NC_000009.11:g.136501861_136501863del , CM000671.1:g.136501861_136501863del GRCh37
NC_000009.10:g.135491682_135491684del NCBI36
NG_008645.1:g.5377_5379del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.333+29_333+31del ENSP00000263611.3:n.333+29_333+31del
ENST00000393056.8:c.339+29_339+31del MANE Select ENSP00000376776.2:n.339+29_339+31del
ENST00000263611.2:c.297+29_297+31del ENSP00000263611.2:n.297+29_297+31del
ENST00000393056.6:c.339+29_339+31del ENSP00000376776.2:n.339+29_339+31del
NM_000787.3:c.339+29_339+31del NP_000778.3:n.339+29_339+31del
NM_000787.4:c.339+29_339+31del MANE Select NP_000778.3:n.339+29_339+31del
Search 100 bp 5'
Search 100 bp 3'