Canonical Allele Identifier: CA1882777271
Gene: DBH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644421G= , CM000671.2:g.133644421G= GRCh38
NC_000009.11:g.136509543G= , CM000671.1:g.136509543G= GRCh37
NC_000009.10:g.135499364G= NCBI36
NG_008645.1:g.13059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.1024+101G= MANE Select ENSP00000376776.2:n.1024+101G=
ENST00000393056.6:c.1024+101G= ENSP00000376776.2:n.1024+101G=
NM_000787.3:c.1024+101G= NP_000778.3:n.1024+101G=
NM_000787.4:c.1024+101G= MANE Select NP_000778.3:n.1024+101G=