Canonical Allele Identifier: CA375409069
Gene: DBH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133639848C>G , CM000671.2:g.133639848C>G GRCh38
NC_000009.11:g.136504970C>G , CM000671.1:g.136504970C>G GRCh37
NC_000009.10:g.135494791C>G NCBI36
NG_008645.1:g.8486C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.334-2359C>G ENSP00000263611.3:n.334-2359C>G
ENST00000393056.8:c.342C>G MANE Select ENSP00000376776.2:p.Asp114Glu
ENST00000263611.2:c.298-2359C>G ENSP00000263611.2:n.298-2359C>G
ENST00000393056.6:c.342C>G ENSP00000376776.2:p.Asp114Glu
NM_000787.3:c.342C>G NP_000778.3:p.Asp114Glu
NM_000787.4:c.342C>G MANE Select NP_000778.3:p.Asp114Glu