Canonical Allele Identifier: CA375415607
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509415C>T (hg19) chr9:g.133644293C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644293C>T , CM000671.2:g.133644293C>T GRCh38
NC_000009.11:g.136509415C>T , CM000671.1:g.136509415C>T GRCh37
NC_000009.10:g.135499236C>T NCBI36
NG_008645.1:g.12931C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.997C>T MANE Select ENSP00000376776.2:p.His333Tyr
ENST00000393056.6:c.997C>T ENSP00000376776.2:p.His333Tyr
NM_000787.3:c.997C>T NP_000778.3:p.His333Tyr
NM_000787.4:c.997C>T MANE Select NP_000778.3:p.His333Tyr
Search 100 bp 5'
Search 100 bp 3'