Canonical Allele Identifier: CA1882770259

Gene: DBH

Linked Data

• dbSNP Id: rs1832081126

Genomic Alleles

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

Transcript Alleles

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