Canonical Allele Identifier: CA860772771
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs573964842
gnomAD v3: 9-133638667-G-T
gnomAD v4: 9-133638667-G-T
MyVariant Identifiers: chr9:g.136503789G>T (hg19) chr9:g.133638667G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638667G>T , CM000671.2:g.133638667G>T GRCh38
NC_000009.11:g.136503789G>T , CM000671.1:g.136503789G>T GRCh37
NC_000009.10:g.135493610G>T NCBI36
NG_008645.1:g.7305G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.333+1957G>T ENSP00000263611.3:n.333+1957G>T
ENST00000393056.8:c.340-1179G>T MANE Select ENSP00000376776.2:n.340-1179G>T
ENST00000263611.2:c.297+1957G>T ENSP00000263611.2:n.297+1957G>T
ENST00000393056.6:c.340-1179G>T ENSP00000376776.2:n.340-1179G>T
NM_000787.3:c.340-1179G>T NP_000778.3:n.340-1179G>T
NM_000787.4:c.340-1179G>T MANE Select NP_000778.3:n.340-1179G>T
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