Canonical Allele Identifier: CA1882770105

Gene: DBH

Linked Data

• dbSNP Id: rs1832079788

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133638637dup , CM000671.2:g.133638637dup	GRCh38
NC_000009.11:g.136503759dup , CM000671.1:g.136503759dup	GRCh37
NC_000009.10:g.135493580dup	NCBI36
NG_008645.1:g.7275dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263611.3:c.333+1927dup	ENSP00000263611.3:n.333+1927dup
ENST00000393056.8:c.340-1209dup MANE Select	ENSP00000376776.2:n.340-1209dup
ENST00000263611.2:c.297+1927dup	ENSP00000263611.2:n.297+1927dup
ENST00000393056.6:c.340-1209dup	ENSP00000376776.2:n.340-1209dup
NM_000787.3:c.340-1209dup	NP_000778.3:n.340-1209dup
NM_000787.4:c.340-1209dup MANE Select	NP_000778.3:n.340-1209dup