Canonical Allele Identifier: CA2839223467

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644352G>T , CM000671.2:g.133644352G>T	GRCh38
NC_000009.11:g.136509474G>T , CM000671.1:g.136509474G>T	GRCh37
NC_000009.10:g.135499295G>T	NCBI36
NG_008645.1:g.12990G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393056.8:c.1024+32G>T MANE Select	ENSP00000376776.2:n.1024+32G>T
ENST00000393056.6:c.1024+32G>T	ENSP00000376776.2:n.1024+32G>T
NM_000787.3:c.1024+32G>T	NP_000778.3:n.1024+32G>T
NM_000787.4:c.1024+32G>T MANE Select	NP_000778.3:n.1024+32G>T