Canonical Allele Identifier: CA467611805
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136501757G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636635G>C , CM000671.2:g.133636635G>C GRCh38
NC_000009.11:g.136501757G>C , CM000671.1:g.136501757G>C GRCh37
NC_000009.10:g.135491578G>C NCBI36
NG_008645.1:g.5273G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.258G>C ENSP00000263611.3:p.Gly86=
ENST00000393056.8:c.264G>C MANE Select ENSP00000376776.2:p.Gly88=
ENST00000263611.2:c.222G>C ENSP00000263611.2:p.Gly74=
ENST00000393056.6:c.264G>C ENSP00000376776.2:p.Gly88=
NM_000787.3:c.264G>C NP_000778.3:p.Gly88=
NM_000787.4:c.264G>C MANE Select NP_000778.3:p.Gly88=