Canonical Allele Identifier: CA918570717
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1564207131
gnomAD v4: 9-133636736-T-TTC
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636736_133636737insTC , CM000671.2:g.133636736_133636737insTC GRCh38
NC_000009.11:g.136501858_136501859insTC , CM000671.1:g.136501858_136501859insTC GRCh37
NC_000009.10:g.135491679_135491680insTC NCBI36
NG_008645.1:g.5374_5375insTC

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+26_333+27insTC ENSP00000263611.3:n.333+26_333+27insTC
ENST00000393056.8:c.339+26_339+27insTC MANE Select ENSP00000376776.2:n.339+26_339+27insTC
ENST00000263611.2:c.297+26_297+27insTC ENSP00000263611.2:n.297+26_297+27insTC
ENST00000393056.6:c.339+26_339+27insTC ENSP00000376776.2:n.339+26_339+27insTC
NM_000787.3:c.339+26_339+27insTC NP_000778.3:n.339+26_339+27insTC
NM_000787.4:c.339+26_339+27insTC MANE Select NP_000778.3:n.339+26_339+27insTC
Search 100 bp 5'
Search 100 bp 3'