Canonical Allele Identifier: CA467613821
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509369T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644247T>A , CM000671.2:g.133644247T>A GRCh38
NC_000009.11:g.136509369T>A , CM000671.1:g.136509369T>A GRCh37
NC_000009.10:g.135499190T>A NCBI36
NG_008645.1:g.12885T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.951T>A MANE Select ENSP00000376776.2:p.Leu317=
ENST00000393056.6:c.951T>A ENSP00000376776.2:p.Leu317=
NM_000787.3:c.951T>A NP_000778.3:p.Leu317=
NM_000787.4:c.951T>A MANE Select NP_000778.3:p.Leu317=
Search 100 bp 5'
Search 100 bp 3'