Canonical Allele Identifier: CA375407770
Gene: DBH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636636A>T , CM000671.2:g.133636636A>T GRCh38
NC_000009.11:g.136501758A>T , CM000671.1:g.136501758A>T GRCh37
NC_000009.10:g.135491579A>T NCBI36
NG_008645.1:g.5274A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.259A>T ENSP00000263611.3:p.Met87Leu
ENST00000393056.8:c.265A>T MANE Select ENSP00000376776.2:p.Met89Leu
ENST00000263611.2:c.223A>T ENSP00000263611.2:p.Met75Leu
ENST00000393056.6:c.265A>T ENSP00000376776.2:p.Met89Leu
NM_000787.3:c.265A>T NP_000778.3:p.Met89Leu
NM_000787.4:c.265A>T MANE Select NP_000778.3:p.Met89Leu