Canonical Allele Identifier: CA860776584
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1305747195
gnomAD v3: 9-133644176-T-A
gnomAD v4: 9-133644176-T-A
MyVariant Identifiers: chr9:g.136509298T>A (hg19) chr9:g.133644176T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644176T>A , CM000671.2:g.133644176T>A GRCh38
NC_000009.11:g.136509298T>A , CM000671.1:g.136509298T>A GRCh37
NC_000009.10:g.135499119T>A NCBI36
NG_008645.1:g.12814T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-42T>A MANE Select ENSP00000376776.2:n.922-42T>A
ENST00000393056.6:c.922-42T>A ENSP00000376776.2:n.922-42T>A
NM_000787.3:c.922-42T>A NP_000778.3:n.922-42T>A
NM_000787.4:c.922-42T>A MANE Select NP_000778.3:n.922-42T>A
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