Canonical Allele Identifier: CA2692393568
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133644422-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644422C>A , CM000671.2:g.133644422C>A GRCh38
NC_000009.11:g.136509544C>A , CM000671.1:g.136509544C>A GRCh37
NC_000009.10:g.135499365C>A NCBI36
NG_008645.1:g.13060C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+102C>A MANE Select ENSP00000376776.2:n.1024+102C>A
ENST00000393056.6:c.1024+102C>A ENSP00000376776.2:n.1024+102C>A
NM_000787.3:c.1024+102C>A NP_000778.3:n.1024+102C>A
NM_000787.4:c.1024+102C>A MANE Select NP_000778.3:n.1024+102C>A
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