Canonical Allele Identifier: CA375415464
Gene: DBH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644272A>G , CM000671.2:g.133644272A>G GRCh38
NC_000009.11:g.136509394A>G , CM000671.1:g.136509394A>G GRCh37
NC_000009.10:g.135499215A>G NCBI36
NG_008645.1:g.12910A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.976A>G MANE Select ENSP00000376776.2:p.Arg326Gly
ENST00000393056.6:c.976A>G ENSP00000376776.2:p.Arg326Gly
NM_000787.3:c.976A>G NP_000778.3:p.Arg326Gly
NM_000787.4:c.976A>G MANE Select NP_000778.3:p.Arg326Gly