Canonical Allele Identifier: CA591066587
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1378333051
gnomAD v2: 9-136501841-C-G
gnomAD v4: 9-133636719-C-G
MyVariant Identifiers: chr9:g.136501841C>G (hg19) chr9:g.133636719C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636719C>G , CM000671.2:g.133636719C>G GRCh38
NC_000009.11:g.136501841C>G , CM000671.1:g.136501841C>G GRCh37
NC_000009.10:g.135491662C>G NCBI36
NG_008645.1:g.5357C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+9C>G ENSP00000263611.3:n.333+9C>G
ENST00000393056.8:c.339+9C>G MANE Select ENSP00000376776.2:n.339+9C>G
ENST00000263611.2:c.297+9C>G ENSP00000263611.2:n.297+9C>G
ENST00000393056.6:c.339+9C>G ENSP00000376776.2:n.339+9C>G
NM_000787.3:c.339+9C>G NP_000778.3:n.339+9C>G
NM_000787.4:c.339+9C>G MANE Select NP_000778.3:n.339+9C>G
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