Canonical Allele Identifier: CA467613962
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509411A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644289A>G , CM000671.2:g.133644289A>G GRCh38
NC_000009.11:g.136509411A>G , CM000671.1:g.136509411A>G GRCh37
NC_000009.10:g.135499232A>G NCBI36
NG_008645.1:g.12927A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.993A>G MANE Select ENSP00000376776.2:p.Glu331=
ENST00000393056.6:c.993A>G ENSP00000376776.2:p.Glu331=
NM_000787.3:c.993A>G NP_000778.3:p.Glu331=
NM_000787.4:c.993A>G MANE Select NP_000778.3:p.Glu331=
Search 100 bp 5'
Search 100 bp 3'