Canonical Allele Identifier: CA375407738
Gene: DBH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636627C>G , CM000671.2:g.133636627C>G GRCh38
NC_000009.11:g.136501749C>G , CM000671.1:g.136501749C>G GRCh37
NC_000009.10:g.135491570C>G NCBI36
NG_008645.1:g.5265C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.250C>G ENSP00000263611.3:p.Leu84Val
ENST00000393056.8:c.256C>G MANE Select ENSP00000376776.2:p.Leu86Val
ENST00000263611.2:c.214C>G ENSP00000263611.2:p.Leu72Val
ENST00000393056.6:c.256C>G ENSP00000376776.2:p.Leu86Val
NM_000787.3:c.256C>G NP_000778.3:p.Leu86Val
NM_000787.4:c.256C>G MANE Select NP_000778.3:p.Leu86Val