Canonical Allele Identifier: CA375407775
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136501759T>G (hg19) chr9:g.133636637T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636637T>G , CM000671.2:g.133636637T>G GRCh38
NC_000009.11:g.136501759T>G , CM000671.1:g.136501759T>G GRCh37
NC_000009.10:g.135491580T>G NCBI36
NG_008645.1:g.5275T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.260T>G ENSP00000263611.3:p.Met87Arg
ENST00000393056.8:c.266T>G MANE Select ENSP00000376776.2:p.Met89Arg
ENST00000263611.2:c.224T>G ENSP00000263611.2:p.Met75Arg
ENST00000393056.6:c.266T>G ENSP00000376776.2:p.Met89Arg
NM_000787.3:c.266T>G NP_000778.3:p.Met89Arg
NM_000787.4:c.266T>G MANE Select NP_000778.3:p.Met89Arg
Search 100 bp 5'
Search 100 bp 3'