Canonical Allele Identifier: CA860776853
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1329024650
gnomAD v4: 9-133644421-G-A
MyVariant Identifiers: chr9:g.136509543G>A (hg19) chr9:g.133644421G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644421G>A , CM000671.2:g.133644421G>A GRCh38
NC_000009.11:g.136509543G>A , CM000671.1:g.136509543G>A GRCh37
NC_000009.10:g.135499364G>A NCBI36
NG_008645.1:g.13059G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+101G>A MANE Select ENSP00000376776.2:n.1024+101G>A
ENST00000393056.6:c.1024+101G>A ENSP00000376776.2:n.1024+101G>A
NM_000787.3:c.1024+101G>A NP_000778.3:n.1024+101G>A
NM_000787.4:c.1024+101G>A MANE Select NP_000778.3:n.1024+101G>A
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