Canonical Allele Identifier: CA1882777269
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644418C= , CM000671.2:g.133644418C= GRCh38
NC_000009.11:g.136509540C= , CM000671.1:g.136509540C= GRCh37
NC_000009.10:g.135499361C= NCBI36
NG_008645.1:g.13056C=

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+98C= MANE Select ENSP00000376776.2:n.1024+98C=
ENST00000393056.6:c.1024+98C= ENSP00000376776.2:n.1024+98C=
NM_000787.3:c.1024+98C= NP_000778.3:n.1024+98C=
NM_000787.4:c.1024+98C= MANE Select NP_000778.3:n.1024+98C=