Canonical Allele Identifier: CA1882777241
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644352G= , CM000671.2:g.133644352G= GRCh38
NC_000009.11:g.136509474G= , CM000671.1:g.136509474G= GRCh37
NC_000009.10:g.135499295G= NCBI36
NG_008645.1:g.12990G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.1024+32G= MANE Select ENSP00000376776.2:n.1024+32G=
ENST00000393056.6:c.1024+32G= ENSP00000376776.2:n.1024+32G=
NM_000787.3:c.1024+32G= NP_000778.3:n.1024+32G=
NM_000787.4:c.1024+32G= MANE Select NP_000778.3:n.1024+32G=
Search 100 bp 5'
Search 100 bp 3'