Canonical Allele Identifier: CA1882777126
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1832153417

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644109del , CM000671.2:g.133644109del GRCh38
NC_000009.11:g.136509231del , CM000671.1:g.136509231del GRCh37
NC_000009.10:g.135499052del NCBI36
NG_008645.1:g.12747del

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-109del MANE Select ENSP00000376776.2:n.922-109del
ENST00000393056.6:c.922-109del ENSP00000376776.2:n.922-109del
NM_000787.3:c.922-109del NP_000778.3:n.922-109del
NM_000787.4:c.922-109del MANE Select NP_000778.3:n.922-109del