Canonical Allele Identifier: CA1882777206
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644264G= , CM000671.2:g.133644264G= GRCh38
NC_000009.11:g.136509386G= , CM000671.1:g.136509386G= GRCh37
NC_000009.10:g.135499207G= NCBI36
NG_008645.1:g.12902G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.968G= MANE Select ENSP00000376776.2:p.Gly323=
ENST00000393056.6:c.968G= ENSP00000376776.2:p.Gly323=
NM_000787.3:c.968G= NP_000778.3:p.Gly323=
NM_000787.4:c.968G= MANE Select NP_000778.3:p.Gly323=