Canonical Allele Identifier: CA1882777268

Gene: DBH

Linked Data

• dbSNP Id: rs1832157654

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644416C>G , CM000671.2:g.133644416C>G	GRCh38
NC_000009.11:g.136509538C>G , CM000671.1:g.136509538C>G	GRCh37
NC_000009.10:g.135499359C>G	NCBI36
NG_008645.1:g.13054C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000393056.8:c.1024+96C>G MANE Select	ENSP00000376776.2:n.1024+96C>G
ENST00000393056.6:c.1024+96C>G	ENSP00000376776.2:n.1024+96C>G
NM_000787.3:c.1024+96C>G	NP_000778.3:n.1024+96C>G
NM_000787.4:c.1024+96C>G MANE Select	NP_000778.3:n.1024+96C>G