Canonical Allele Identifier: CA1882770191

Gene: DBH

Linked Data

• dbSNP Id: rs1832080632

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133638696del , CM000671.2:g.133638696del	GRCh38
NC_000009.11:g.136503818del , CM000671.1:g.136503818del	GRCh37
NC_000009.10:g.135493639del	NCBI36
NG_008645.1:g.7334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263611.3:c.333+1986del	ENSP00000263611.3:n.333+1986del
ENST00000393056.8:c.340-1150del MANE Select	ENSP00000376776.2:n.340-1150del
ENST00000263611.2:c.297+1986del	ENSP00000263611.2:n.297+1986del
ENST00000393056.6:c.340-1150del	ENSP00000376776.2:n.340-1150del
NM_000787.3:c.340-1150del	NP_000778.3:n.340-1150del
NM_000787.4:c.340-1150del MANE Select	NP_000778.3:n.340-1150del