Canonical Allele Identifier: CA2720459359
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs754138272
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636725C>A , CM000671.2:g.133636725C>A GRCh38
NC_000009.11:g.136501847C>A , CM000671.1:g.136501847C>A GRCh37
NC_000009.10:g.135491668C>A NCBI36
NG_008645.1:g.5363C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+15C>A ENSP00000263611.3:n.333+15C>A
ENST00000393056.8:c.339+15C>A MANE Select ENSP00000376776.2:n.339+15C>A
ENST00000263611.2:c.297+15C>A ENSP00000263611.2:n.297+15C>A
ENST00000393056.6:c.339+15C>A ENSP00000376776.2:n.339+15C>A
NM_000787.3:c.339+15C>A NP_000778.3:n.339+15C>A
NM_000787.4:c.339+15C>A MANE Select NP_000778.3:n.339+15C>A
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