Canonical Allele Identifier: CA1882768036

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133636629G= , CM000671.2:g.133636629G=	GRCh38
NC_000009.11:g.136501751G= , CM000671.1:g.136501751G=	GRCh37
NC_000009.10:g.135491572G=	NCBI36
NG_008645.1:g.5267G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263611.3:c.252G=	ENSP00000263611.3:p.Leu84=
ENST00000393056.8:c.258G= MANE Select	ENSP00000376776.2:p.Leu86=
ENST00000263611.2:c.216G=	ENSP00000263611.2:p.Leu72=
ENST00000393056.6:c.258G=	ENSP00000376776.2:p.Leu86=
NM_000787.3:c.258G=	NP_000778.3:p.Leu86=
NM_000787.4:c.258G= MANE Select	NP_000778.3:p.Leu86=