Canonical Allele Identifier: CA375415508
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs142042694
MyVariant Identifiers: chr9:g.136509399T>G (hg19) chr9:g.133644277T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644277T>G , CM000671.2:g.133644277T>G GRCh38
NC_000009.11:g.136509399T>G , CM000671.1:g.136509399T>G GRCh37
NC_000009.10:g.135499220T>G NCBI36
NG_008645.1:g.12915T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.981T>G MANE Select ENSP00000376776.2:p.Tyr327Ter
ENST00000393056.6:c.981T>G ENSP00000376776.2:p.Tyr327Ter
NM_000787.3:c.981T>G NP_000778.3:p.Tyr327Ter
NM_000787.4:c.981T>G MANE Select NP_000778.3:p.Tyr327Ter
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