Canonical Allele Identifier: CA200957455
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1029549121
gnomAD v2: 9-136503843-G-C
gnomAD v3: 9-133638721-G-C
gnomAD v4: 9-133638721-G-C
MyVariant Identifiers: chr9:g.136503843G>C (hg19) chr9:g.133638721G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638721G>C , CM000671.2:g.133638721G>C GRCh38
NC_000009.11:g.136503843G>C , CM000671.1:g.136503843G>C GRCh37
NC_000009.10:g.135493664G>C NCBI36
NG_008645.1:g.7359G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+2011G>C ENSP00000263611.3:n.333+2011G>C
ENST00000393056.8:c.340-1125G>C MANE Select ENSP00000376776.2:n.340-1125G>C
ENST00000263611.2:c.297+2011G>C ENSP00000263611.2:n.297+2011G>C
ENST00000393056.6:c.340-1125G>C ENSP00000376776.2:n.340-1125G>C
NM_000787.3:c.340-1125G>C NP_000778.3:n.340-1125G>C
NM_000787.4:c.340-1125G>C MANE Select NP_000778.3:n.340-1125G>C
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