Canonical Allele Identifier: CA375415184
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509348C>G (hg19) chr9:g.133644226C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644226C>G , CM000671.2:g.133644226C>G GRCh38
NC_000009.11:g.136509348C>G , CM000671.1:g.136509348C>G GRCh37
NC_000009.10:g.135499169C>G NCBI36
NG_008645.1:g.12864C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.930C>G MANE Select ENSP00000376776.2:p.Tyr310Ter
ENST00000393056.6:c.930C>G ENSP00000376776.2:p.Tyr310Ter
NM_000787.3:c.930C>G NP_000778.3:p.Tyr310Ter
NM_000787.4:c.930C>G MANE Select NP_000778.3:p.Tyr310Ter
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Search 100 bp 3'