Canonical Allele Identifier: CA2692393455
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133644159-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644162del , CM000671.2:g.133644162del GRCh38
NC_000009.11:g.136509284del , CM000671.1:g.136509284del GRCh37
NC_000009.10:g.135499105del NCBI36
NG_008645.1:g.12800del

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-56del MANE Select ENSP00000376776.2:n.922-56del
ENST00000393056.6:c.922-56del ENSP00000376776.2:n.922-56del
NM_000787.3:c.922-56del NP_000778.3:n.922-56del
NM_000787.4:c.922-56del MANE Select NP_000778.3:n.922-56del
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Search 100 bp 3'