Canonical Allele Identifier: CA1882777184
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644215_133644216delinsCA , CM000671.2:g.133644215_133644216delinsCA GRCh38
NC_000009.11:g.136509337_136509338delinsCA , CM000671.1:g.136509337_136509338delinsCA GRCh37
NC_000009.10:g.135499158_135499159delinsCA NCBI36
NG_008645.1:g.12853_12854delinsCA

Transcript Alleles

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