Canonical Allele Identifier: CA2840903956

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644335T>A , CM000671.2:g.133644335T>A	GRCh38
NC_000009.11:g.136509457T>A , CM000671.1:g.136509457T>A	GRCh37
NC_000009.10:g.135499278T>A	NCBI36
NG_008645.1:g.12973T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393056.8:c.1024+15T>A MANE Select	ENSP00000376776.2:n.1024+15T>A
ENST00000393056.6:c.1024+15T>A	ENSP00000376776.2:n.1024+15T>A
NM_000787.3:c.1024+15T>A	NP_000778.3:n.1024+15T>A
NM_000787.4:c.1024+15T>A MANE Select	NP_000778.3:n.1024+15T>A