Canonical Allele Identifier: CA1882770233

Gene: DBH

Linked Data

• dbSNP Id: rs1832080904

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133638733_133638734del , CM000671.2:g.133638733_133638734del	GRCh38
NC_000009.11:g.136503855_136503856del , CM000671.1:g.136503855_136503856del	GRCh37
NC_000009.10:g.135493676_135493677del	NCBI36
NG_008645.1:g.7371_7372del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263611.3:c.333+2023_333+2024del	ENSP00000263611.3:n.333+2023_333+2024del
ENST00000393056.8:c.340-1113_340-1112del MANE Select	ENSP00000376776.2:n.340-1113_340-1112del
ENST00000263611.2:c.297+2023_297+2024del	ENSP00000263611.2:n.297+2023_297+2024del
ENST00000393056.6:c.340-1113_340-1112del	ENSP00000376776.2:n.340-1113_340-1112del
NM_000787.3:c.340-1113_340-1112del	NP_000778.3:n.340-1113_340-1112del
NM_000787.4:c.340-1113_340-1112del MANE Select	NP_000778.3:n.340-1113_340-1112del