Canonical Allele Identifier: CA375415398
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs756772568
MyVariant Identifiers: chr9:g.136509380G>T (hg19) chr9:g.133644258G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644258G>T , CM000671.2:g.133644258G>T GRCh38
NC_000009.11:g.136509380G>T , CM000671.1:g.136509380G>T GRCh37
NC_000009.10:g.135499201G>T NCBI36
NG_008645.1:g.12896G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.962G>T MANE Select ENSP00000376776.2:p.Gly321Val
ENST00000393056.6:c.962G>T ENSP00000376776.2:p.Gly321Val
NM_000787.3:c.962G>T NP_000778.3:p.Gly321Val
NM_000787.4:c.962G>T MANE Select NP_000778.3:p.Gly321Val
Search 100 bp 5'
Search 100 bp 3'