Canonical Allele Identifier: CA1882770231
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638730_133638732delinsACT , CM000671.2:g.133638730_133638732delinsACT GRCh38
NC_000009.11:g.136503852_136503854delinsACT , CM000671.1:g.136503852_136503854delinsACT GRCh37
NC_000009.10:g.135493673_135493675delinsACT NCBI36
NG_008645.1:g.7368_7370delinsACT

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+2020_333+2022delinsACT ENSP00000263611.3:n.333+2020_333+2022deli...
ENST00000393056.8:c.340-1116_340-1114delinsACT MANE Select ENSP00000376776.2:n.340-1116_340-1114deli...
ENST00000263611.2:c.297+2020_297+2022delinsACT ENSP00000263611.2:n.297+2020_297+2022deli...
ENST00000393056.6:c.340-1116_340-1114delinsACT ENSP00000376776.2:n.340-1116_340-1114deli...
NM_000787.3:c.340-1116_340-1114delinsACT NP_000778.3:n.340-1116_340-1114delinsACT
NM_000787.4:c.340-1116_340-1114delinsACT MANE Select NP_000778.3:n.340-1116_340-1114delinsACT