Canonical Allele Identifier: CA467611779
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133636626-C-G
MyVariant Identifiers: chr9:g.136501748C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636626C>G , CM000671.2:g.133636626C>G GRCh38
NC_000009.11:g.136501748C>G , CM000671.1:g.136501748C>G GRCh37
NC_000009.10:g.135491569C>G NCBI36
NG_008645.1:g.5264C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.249C>G ENSP00000263611.3:p.Val83=
ENST00000393056.8:c.255C>G MANE Select ENSP00000376776.2:p.Val85=
ENST00000263611.2:c.213C>G ENSP00000263611.2:p.Val71=
ENST00000393056.6:c.255C>G ENSP00000376776.2:p.Val85=
NM_000787.3:c.255C>G NP_000778.3:p.Val85=
NM_000787.4:c.255C>G MANE Select NP_000778.3:p.Val85=
Search 100 bp 5'
Search 100 bp 3'