Canonical Allele Identifier: CA467613813
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133644244-C-T
MyVariant Identifiers: chr9:g.136509366C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644244C>T , CM000671.2:g.133644244C>T GRCh38
NC_000009.11:g.136509366C>T , CM000671.1:g.136509366C>T GRCh37
NC_000009.10:g.135499187C>T NCBI36
NG_008645.1:g.12882C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.948C>T MANE Select ENSP00000376776.2:p.Gly316=
ENST00000393056.6:c.948C>T ENSP00000376776.2:p.Gly316=
NM_000787.3:c.948C>T NP_000778.3:p.Gly316=
NM_000787.4:c.948C>T MANE Select NP_000778.3:p.Gly316=
Search 100 bp 5'
Search 100 bp 3'