Canonical Allele Identifier: CA1882777178
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644205T= , CM000671.2:g.133644205T= GRCh38
NC_000009.11:g.136509327T= , CM000671.1:g.136509327T= GRCh37
NC_000009.10:g.135499148T= NCBI36
NG_008645.1:g.12843T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-13T= MANE Select ENSP00000376776.2:n.922-13T=
ENST00000393056.6:c.922-13T= ENSP00000376776.2:n.922-13T=
NM_000787.3:c.922-13T= NP_000778.3:n.922-13T=
NM_000787.4:c.922-13T= MANE Select NP_000778.3:n.922-13T=