Canonical Allele Identifier: CA375407768
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136501758A>G (hg19) chr9:g.133636636A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636636A>G , CM000671.2:g.133636636A>G GRCh38
NC_000009.11:g.136501758A>G , CM000671.1:g.136501758A>G GRCh37
NC_000009.10:g.135491579A>G NCBI36
NG_008645.1:g.5274A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.259A>G ENSP00000263611.3:p.Met87Val
ENST00000393056.8:c.265A>G MANE Select ENSP00000376776.2:p.Met89Val
ENST00000263611.2:c.223A>G ENSP00000263611.2:p.Met75Val
ENST00000393056.6:c.265A>G ENSP00000376776.2:p.Met89Val
NM_000787.3:c.265A>G NP_000778.3:p.Met89Val
NM_000787.4:c.265A>G MANE Select NP_000778.3:p.Met89Val
Search 100 bp 5'
Search 100 bp 3'