Canonical Allele Identifier: CA200963760
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs201624659
gnomAD v4: 9-133644159-G-GC
MyVariant Identifiers: chr9:g.136509281_136509282insC (hg19) chr9:g.133644159_133644160insC (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-56dup MANE Select ENSP00000376776.2:n.922-56dup
ENST00000393056.6:c.922-56dup ENSP00000376776.2:n.922-56dup
NM_000787.3:c.922-56dup NP_000778.3:n.922-56dup
NM_000787.4:c.922-56dup MANE Select NP_000778.3:n.922-56dup
Search 100 bp 5'
Search 100 bp 3'