Canonical Allele Identifier: CA1882777270
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644420C= , CM000671.2:g.133644420C= GRCh38
NC_000009.11:g.136509542C= , CM000671.1:g.136509542C= GRCh37
NC_000009.10:g.135499363C= NCBI36
NG_008645.1:g.13058C=

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+100C= MANE Select ENSP00000376776.2:n.1024+100C=
ENST00000393056.6:c.1024+100C= ENSP00000376776.2:n.1024+100C=
NM_000787.3:c.1024+100C= NP_000778.3:n.1024+100C=
NM_000787.4:c.1024+100C= MANE Select NP_000778.3:n.1024+100C=