Canonical Allele Identifier: CA375407761

Gene: DBH

Linked Data

• MyVariant Identifiers: chr9:g.136501756G>T (hg19) ; chr9:g.133636634G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133636634G>T , CM000671.2:g.133636634G>T	GRCh38
NC_000009.11:g.136501756G>T , CM000671.1:g.136501756G>T	GRCh37
NC_000009.10:g.135491577G>T	NCBI36
NG_008645.1:g.5272G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263611.3:c.257G>T	ENSP00000263611.3:p.Gly86Val
ENST00000393056.8:c.263G>T MANE Select	ENSP00000376776.2:p.Gly88Val
ENST00000263611.2:c.221G>T	ENSP00000263611.2:p.Gly74Val
ENST00000393056.6:c.263G>T	ENSP00000376776.2:p.Gly88Val
NM_000787.3:c.263G>T	NP_000778.3:p.Gly88Val
NM_000787.4:c.263G>T MANE Select	NP_000778.3:p.Gly88Val