Canonical Allele Identifier: CA5313467
Community Standard Title: NM_000787.4(DBH):c.1365G>A (p.Ser455=)
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133652275G>A , CM000671.2:g.133652275G>A GRCh38
NC_000009.11:g.136517397G>A , CM000671.1:g.136517397G>A GRCh37
NC_000009.10:g.135507218G>A NCBI36
NG_008645.1:g.20913G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000787.4:c.1365G>A MANE Select NP_000778.3:p.Ser455=
ENST00000393056.8:c.1365G>A MANE Select ENSP00000376776.2:p.Ser455=
NM_000787.3:c.1365G>A NP_000778.3:p.Ser455=
ENST00000393056.6:c.1365G>A ENSP00000376776.2:p.Ser455=
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