Canonical Allele Identifier: CA591066734
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1191010784
gnomAD v2: 9-136503797-A-G
gnomAD v3: 9-133638675-A-G
gnomAD v4: 9-133638675-A-G
MyVariant Identifiers: chr9:g.136503797A>G (hg19) chr9:g.133638675A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638675A>G , CM000671.2:g.133638675A>G GRCh38
NC_000009.11:g.136503797A>G , CM000671.1:g.136503797A>G GRCh37
NC_000009.10:g.135493618A>G NCBI36
NG_008645.1:g.7313A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.333+1965A>G ENSP00000263611.3:n.333+1965A>G
ENST00000393056.8:c.340-1171A>G MANE Select ENSP00000376776.2:n.340-1171A>G
ENST00000263611.2:c.297+1965A>G ENSP00000263611.2:n.297+1965A>G
ENST00000393056.6:c.340-1171A>G ENSP00000376776.2:n.340-1171A>G
NM_000787.3:c.340-1171A>G NP_000778.3:n.340-1171A>G
NM_000787.4:c.340-1171A>G MANE Select NP_000778.3:n.340-1171A>G
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