Canonical Allele Identifier: CA375415552
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1588348769
MyVariant Identifiers: chr9:g.136509406C>G (hg19) chr9:g.133644284C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644284C>G , CM000671.2:g.133644284C>G GRCh38
NC_000009.11:g.136509406C>G , CM000671.1:g.136509406C>G GRCh37
NC_000009.10:g.135499227C>G NCBI36
NG_008645.1:g.12922C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.988C>G MANE Select ENSP00000376776.2:p.Leu330Val
ENST00000393056.6:c.988C>G ENSP00000376776.2:p.Leu330Val
NM_000787.3:c.988C>G NP_000778.3:p.Leu330Val
NM_000787.4:c.988C>G MANE Select NP_000778.3:p.Leu330Val
Search 100 bp 5'
Search 100 bp 3'