Canonical Allele Identifier: CA5313256
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs756772568

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644258G>A , CM000671.2:g.133644258G>A GRCh38
NC_000009.11:g.136509380G>A , CM000671.1:g.136509380G>A GRCh37
NC_000009.10:g.135499201G>A NCBI36
NG_008645.1:g.12896G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.962G>A MANE Select ENSP00000376776.2:p.Gly321Asp
ENST00000393056.6:c.962G>A ENSP00000376776.2:p.Gly321Asp
NM_000787.3:c.962G>A NP_000778.3:p.Gly321Asp
NM_000787.4:c.962G>A MANE Select NP_000778.3:p.Gly321Asp