Canonical Allele Identifier: CA1882777145
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644139A= , CM000671.2:g.133644139A= GRCh38
NC_000009.11:g.136509261A= , CM000671.1:g.136509261A= GRCh37
NC_000009.10:g.135499082A= NCBI36
NG_008645.1:g.12777A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-79A= MANE Select ENSP00000376776.2:n.922-79A=
ENST00000393056.6:c.922-79A= ENSP00000376776.2:n.922-79A=
NM_000787.3:c.922-79A= NP_000778.3:n.922-79A=
NM_000787.4:c.922-79A= MANE Select NP_000778.3:n.922-79A=