Canonical Allele Identifier: CA200964160
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs879016439
gnomAD v4: 9-133644465-C-G
MyVariant Identifiers: chr9:g.136509587C>G (hg19) chr9:g.133644465C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644465C>G , CM000671.2:g.133644465C>G GRCh38
NC_000009.11:g.136509587C>G , CM000671.1:g.136509587C>G GRCh37
NC_000009.10:g.135499408C>G NCBI36
NG_008645.1:g.13103C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.1024+145C>G MANE Select ENSP00000376776.2:n.1024+145C>G
ENST00000393056.6:c.1024+145C>G ENSP00000376776.2:n.1024+145C>G
NM_000787.3:c.1024+145C>G NP_000778.3:n.1024+145C>G
NM_000787.4:c.1024+145C>G MANE Select NP_000778.3:n.1024+145C>G
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