Canonical Allele Identifier: CA1882777267

Gene: DBH

Genomic Alleles

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

Transcript Alleles

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