Canonical Allele Identifier: CA1882770167

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133638689C= , CM000671.2:g.133638689C=	GRCh38
NC_000009.11:g.136503811C= , CM000671.1:g.136503811C=	GRCh37
NC_000009.10:g.135493632C=	NCBI36
NG_008645.1:g.7327C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263611.3:c.333+1979C=	ENSP00000263611.3:n.333+1979C=
ENST00000393056.8:c.340-1157C= MANE Select	ENSP00000376776.2:n.340-1157C=
ENST00000263611.2:c.297+1979C=	ENSP00000263611.2:n.297+1979C=
ENST00000393056.6:c.340-1157C=	ENSP00000376776.2:n.340-1157C=
NM_000787.3:c.340-1157C=	NP_000778.3:n.340-1157C=
NM_000787.4:c.340-1157C= MANE Select	NP_000778.3:n.340-1157C=