Canonical Allele Identifier: CA2562096827
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644100C>G , CM000671.2:g.133644100C>G GRCh38
NC_000009.11:g.136509222C>G , CM000671.1:g.136509222C>G GRCh37
NC_000009.10:g.135499043C>G NCBI36
NG_008645.1:g.12738C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-118C>G MANE Select ENSP00000376776.2:n.922-118C>G
ENST00000393056.6:c.922-118C>G ENSP00000376776.2:n.922-118C>G
NM_000787.3:c.922-118C>G NP_000778.3:n.922-118C>G
NM_000787.4:c.922-118C>G MANE Select NP_000778.3:n.922-118C>G
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