Canonical Allele Identifier: CA1882770247
Gene: DBH HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638743G= , CM000671.2:g.133638743G= GRCh38
NC_000009.11:g.136503865G= , CM000671.1:g.136503865G= GRCh37
NC_000009.10:g.135493686G= NCBI36
NG_008645.1:g.7381G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+2033G= ENSP00000263611.3:n.333+2033G=
ENST00000393056.8:c.340-1103G= MANE Select ENSP00000376776.2:n.340-1103G=
ENST00000263611.2:c.297+2033G= ENSP00000263611.2:n.297+2033G=
ENST00000393056.6:c.340-1103G= ENSP00000376776.2:n.340-1103G=
NM_000787.3:c.340-1103G= NP_000778.3:n.340-1103G=
NM_000787.4:c.340-1103G= MANE Select NP_000778.3:n.340-1103G=
Search 100 bp 5'
Search 100 bp 3'