Canonical Allele Identifier: CA200963924
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs76010730
MyVariant Identifiers: chr9:g.136509393C>T (hg19) chr9:g.133644271C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644271C>T , CM000671.2:g.133644271C>T GRCh38
NC_000009.11:g.136509393C>T , CM000671.1:g.136509393C>T GRCh37
NC_000009.10:g.135499214C>T NCBI36
NG_008645.1:g.12909C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.975C>T MANE Select ENSP00000376776.2:p.Ser325=
ENST00000393056.6:c.975C>T ENSP00000376776.2:p.Ser325=
NM_000787.3:c.975C>T NP_000778.3:p.Ser325=
NM_000787.4:c.975C>T MANE Select NP_000778.3:p.Ser325=
Search 100 bp 5'
Search 100 bp 3'