Canonical Allele Identifier: CA375415566

Gene: DBH

Linked Data

• MyVariant Identifiers: chr9:g.136509409G>C (hg19) ; chr9:g.133644287G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644287G>C , CM000671.2:g.133644287G>C	GRCh38
NC_000009.11:g.136509409G>C , CM000671.1:g.136509409G>C	GRCh37
NC_000009.10:g.135499230G>C	NCBI36
NG_008645.1:g.12925G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393056.8:c.991G>C MANE Select	ENSP00000376776.2:p.Glu331Gln
ENST00000393056.6:c.991G>C	ENSP00000376776.2:p.Glu331Gln
NM_000787.3:c.991G>C	NP_000778.3:p.Glu331Gln
NM_000787.4:c.991G>C MANE Select	NP_000778.3:p.Glu331Gln