Canonical Allele Identifier: CA375415408
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509382C>T (hg19) chr9:g.133644260C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644260C>T , CM000671.2:g.133644260C>T GRCh38
NC_000009.11:g.136509382C>T , CM000671.1:g.136509382C>T GRCh37
NC_000009.10:g.135499203C>T NCBI36
NG_008645.1:g.12898C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.964C>T MANE Select ENSP00000376776.2:p.Pro322Ser
ENST00000393056.6:c.964C>T ENSP00000376776.2:p.Pro322Ser
NM_000787.3:c.964C>T NP_000778.3:p.Pro322Ser
NM_000787.4:c.964C>T MANE Select NP_000778.3:p.Pro322Ser
Search 100 bp 5'
Search 100 bp 3'