Canonical Allele Identifier: CA1882777191
Gene: DBH HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644237A= , CM000671.2:g.133644237A= GRCh38
NC_000009.11:g.136509359A= , CM000671.1:g.136509359A= GRCh37
NC_000009.10:g.135499180A= NCBI36
NG_008645.1:g.12875A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.941A= MANE Select ENSP00000376776.2:p.Glu314=
ENST00000393056.6:c.941A= ENSP00000376776.2:p.Glu314=
NM_000787.3:c.941A= NP_000778.3:p.Glu314=
NM_000787.4:c.941A= MANE Select NP_000778.3:p.Glu314=
Search 100 bp 5'
Search 100 bp 3'