Canonical Allele Identifier: CA1882777196
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644246T= , CM000671.2:g.133644246T= GRCh38
NC_000009.11:g.136509368T= , CM000671.1:g.136509368T= GRCh37
NC_000009.10:g.135499189T= NCBI36
NG_008645.1:g.12884T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.950T= MANE Select ENSP00000376776.2:p.Leu317=
ENST00000393056.6:c.950T= ENSP00000376776.2:p.Leu317=
NM_000787.3:c.950T= NP_000778.3:p.Leu317=
NM_000787.4:c.950T= MANE Select NP_000778.3:p.Leu317=
Search 100 bp 5'
Search 100 bp 3'