Canonical Allele Identifier: CA860776543
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1237401309
gnomAD v4: 9-133644084-C-A
MyVariant Identifiers: chr9:g.136509206C>A (hg19) chr9:g.133644084C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644084C>A , CM000671.2:g.133644084C>A GRCh38
NC_000009.11:g.136509206C>A , CM000671.1:g.136509206C>A GRCh37
NC_000009.10:g.135499027C>A NCBI36
NG_008645.1:g.12722C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-134C>A MANE Select ENSP00000376776.2:n.922-134C>A
ENST00000393056.6:c.922-134C>A ENSP00000376776.2:n.922-134C>A
NM_000787.3:c.922-134C>A NP_000778.3:n.922-134C>A
NM_000787.4:c.922-134C>A MANE Select NP_000778.3:n.922-134C>A
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