Canonical Allele Identifier: CA1882777207
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644266T= , CM000671.2:g.133644266T= GRCh38
NC_000009.11:g.136509388T= , CM000671.1:g.136509388T= GRCh37
NC_000009.10:g.135499209T= NCBI36
NG_008645.1:g.12904T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.970T= MANE Select ENSP00000376776.2:p.Ser324=
ENST00000393056.6:c.970T= ENSP00000376776.2:p.Ser324=
NM_000787.3:c.970T= NP_000778.3:p.Ser324=
NM_000787.4:c.970T= MANE Select NP_000778.3:p.Ser324=