Canonical Allele Identifier: CA1882777125
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644104_133644105delinsGC , CM000671.2:g.133644104_133644105delinsGC GRCh38
NC_000009.11:g.136509226_136509227delinsGC , CM000671.1:g.136509226_136509227delinsGC GRCh37
NC_000009.10:g.135499047_135499048delinsGC NCBI36
NG_008645.1:g.12742_12743delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-114_922-113delinsGC MANE Select ENSP00000376776.2:n.922-114_922-113delinsGC
ENST00000393056.6:c.922-114_922-113delinsGC ENSP00000376776.2:n.922-114_922-113delinsGC
NM_000787.3:c.922-114_922-113delinsGC NP_000778.3:n.922-114_922-113delinsGC
NM_000787.4:c.922-114_922-113delinsGC MANE Select NP_000778.3:n.922-114_922-113delinsGC