Canonical Allele Identifier: CA2692393479
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133644196-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644196T>C , CM000671.2:g.133644196T>C GRCh38
NC_000009.11:g.136509318T>C , CM000671.1:g.136509318T>C GRCh37
NC_000009.10:g.135499139T>C NCBI36
NG_008645.1:g.12834T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-22T>C MANE Select ENSP00000376776.2:n.922-22T>C
ENST00000393056.6:c.922-22T>C ENSP00000376776.2:n.922-22T>C
NM_000787.3:c.922-22T>C NP_000778.3:n.922-22T>C
NM_000787.4:c.922-22T>C MANE Select NP_000778.3:n.922-22T>C
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