Canonical Allele Identifier: CA1882770112
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638641C= , CM000671.2:g.133638641C= GRCh38
NC_000009.11:g.136503763C= , CM000671.1:g.136503763C= GRCh37
NC_000009.10:g.135493584C= NCBI36
NG_008645.1:g.7279C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263611.3:c.333+1931C= ENSP00000263611.3:n.333+1931C=
ENST00000393056.8:c.340-1205C= MANE Select ENSP00000376776.2:n.340-1205C=
ENST00000263611.2:c.297+1931C= ENSP00000263611.2:n.297+1931C=
ENST00000393056.6:c.340-1205C= ENSP00000376776.2:n.340-1205C=
NM_000787.3:c.340-1205C= NP_000778.3:n.340-1205C=
NM_000787.4:c.340-1205C= MANE Select NP_000778.3:n.340-1205C=
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