Canonical Allele Identifier: CA1882777162
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644182_133644184delinsGAC , CM000671.2:g.133644182_133644184delinsGAC GRCh38
NC_000009.11:g.136509304_136509306delinsGAC , CM000671.1:g.136509304_136509306delinsGAC GRCh37
NC_000009.10:g.135499125_135499127delinsGAC NCBI36
NG_008645.1:g.12820_12822delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-36_922-34delinsGAC MANE Select ENSP00000376776.2:n.922-36_922-34delinsGAC
ENST00000393056.6:c.922-36_922-34delinsGAC ENSP00000376776.2:n.922-36_922-34delinsGAC
NM_000787.3:c.922-36_922-34delinsGAC NP_000778.3:n.922-36_922-34delinsGAC
NM_000787.4:c.922-36_922-34delinsGAC MANE Select NP_000778.3:n.922-36_922-34delinsGAC