Canonical Allele Identifier: CA1882770190
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638696_133638697delinsGT , CM000671.2:g.133638696_133638697delinsGT GRCh38
NC_000009.11:g.136503818_136503819delinsGT , CM000671.1:g.136503818_136503819delinsGT GRCh37
NC_000009.10:g.135493639_135493640delinsGT NCBI36
NG_008645.1:g.7334_7335delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+1986_333+1987delinsGT ENSP00000263611.3:n.333+1986_333+1987deli...
ENST00000393056.8:c.340-1150_340-1149delinsGT MANE Select ENSP00000376776.2:n.340-1150_340-1149deli...
ENST00000263611.2:c.297+1986_297+1987delinsGT ENSP00000263611.2:n.297+1986_297+1987deli...
ENST00000393056.6:c.340-1150_340-1149delinsGT ENSP00000376776.2:n.340-1150_340-1149deli...
NM_000787.3:c.340-1150_340-1149delinsGT NP_000778.3:n.340-1150_340-1149delinsGT
NM_000787.4:c.340-1150_340-1149delinsGT MANE Select NP_000778.3:n.340-1150_340-1149delinsGT