Canonical Allele Identifier: CA1882768042
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636630T= , CM000671.2:g.133636630T= GRCh38
NC_000009.11:g.136501752T= , CM000671.1:g.136501752T= GRCh37
NC_000009.10:g.135491573T= NCBI36
NG_008645.1:g.5268T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.253T= ENSP00000263611.3:p.Phe85=
ENST00000393056.8:c.259T= MANE Select ENSP00000376776.2:p.Phe87=
ENST00000263611.2:c.217T= ENSP00000263611.2:p.Phe73=
ENST00000393056.6:c.259T= ENSP00000376776.2:p.Phe87=
NM_000787.3:c.259T= NP_000778.3:p.Phe87=
NM_000787.4:c.259T= MANE Select NP_000778.3:p.Phe87=