Canonical Allele Identifier: CA375415161

Gene: DBH

Linked Data

• MyVariant Identifiers: chr9:g.136509344T>C (hg19) ; chr9:g.133644222T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644222T>C , CM000671.2:g.133644222T>C	GRCh38
NC_000009.11:g.136509344T>C , CM000671.1:g.136509344T>C	GRCh37
NC_000009.10:g.135499165T>C	NCBI36
NG_008645.1:g.12860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393056.8:c.926T>C MANE Select	ENSP00000376776.2:p.Phe309Ser
ENST00000393056.6:c.926T>C	ENSP00000376776.2:p.Phe309Ser
NM_000787.3:c.926T>C	NP_000778.3:p.Phe309Ser
NM_000787.4:c.926T>C MANE Select	NP_000778.3:p.Phe309Ser