Canonical Allele Identifier: CA1882770258

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133638758C= , CM000671.2:g.133638758C=	GRCh38
NC_000009.11:g.136503880C= , CM000671.1:g.136503880C=	GRCh37
NC_000009.10:g.135493701C=	NCBI36
NG_008645.1:g.7396C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263611.3:c.333+2048C=	ENSP00000263611.3:n.333+2048C=
ENST00000393056.8:c.340-1088C= MANE Select	ENSP00000376776.2:n.340-1088C=
ENST00000263611.2:c.297+2048C=	ENSP00000263611.2:n.297+2048C=
ENST00000393056.6:c.340-1088C=	ENSP00000376776.2:n.340-1088C=
NM_000787.3:c.340-1088C=	NP_000778.3:n.340-1088C=
NM_000787.4:c.340-1088C= MANE Select	NP_000778.3:n.340-1088C=