Canonical Allele Identifier: CA1882768048

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133636631T= , CM000671.2:g.133636631T=	GRCh38
NC_000009.11:g.136501753T= , CM000671.1:g.136501753T=	GRCh37
NC_000009.10:g.135491574T=	NCBI36
NG_008645.1:g.5269T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263611.3:c.254T=	ENSP00000263611.3:p.Phe85=
ENST00000393056.8:c.260T= MANE Select	ENSP00000376776.2:p.Phe87=
ENST00000263611.2:c.218T=	ENSP00000263611.2:p.Phe73=
ENST00000393056.6:c.260T=	ENSP00000376776.2:p.Phe87=
NM_000787.3:c.260T=	NP_000778.3:p.Phe87=
NM_000787.4:c.260T= MANE Select	NP_000778.3:p.Phe87=