Canonical Allele Identifier: CA375407773
Gene: DBH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636637T>C , CM000671.2:g.133636637T>C GRCh38
NC_000009.11:g.136501759T>C , CM000671.1:g.136501759T>C GRCh37
NC_000009.10:g.135491580T>C NCBI36
NG_008645.1:g.5275T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.260T>C ENSP00000263611.3:p.Met87Thr
ENST00000393056.8:c.266T>C MANE Select ENSP00000376776.2:p.Met89Thr
ENST00000263611.2:c.224T>C ENSP00000263611.2:p.Met75Thr
ENST00000393056.6:c.266T>C ENSP00000376776.2:p.Met89Thr
NM_000787.3:c.266T>C NP_000778.3:p.Met89Thr
NM_000787.4:c.266T>C MANE Select NP_000778.3:p.Met89Thr