Canonical Allele Identifier: CA375415622
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509418T>A (hg19) chr9:g.133644296T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644296T>A , CM000671.2:g.133644296T>A GRCh38
NC_000009.11:g.136509418T>A , CM000671.1:g.136509418T>A GRCh37
NC_000009.10:g.135499239T>A NCBI36
NG_008645.1:g.12934T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.1000T>A MANE Select ENSP00000376776.2:p.Tyr334Asn
ENST00000393056.6:c.1000T>A ENSP00000376776.2:p.Tyr334Asn
NM_000787.3:c.1000T>A NP_000778.3:p.Tyr334Asn
NM_000787.4:c.1000T>A MANE Select NP_000778.3:p.Tyr334Asn
Search 100 bp 5'
Search 100 bp 3'