Canonical Allele Identifier: CA1882777150
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1832154180
gnomAD v4: 9-133644157-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644157C>T , CM000671.2:g.133644157C>T GRCh38
NC_000009.11:g.136509279C>T , CM000671.1:g.136509279C>T GRCh37
NC_000009.10:g.135499100C>T NCBI36
NG_008645.1:g.12795C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-61C>T MANE Select ENSP00000376776.2:n.922-61C>T
ENST00000393056.6:c.922-61C>T ENSP00000376776.2:n.922-61C>T
NM_000787.3:c.922-61C>T NP_000778.3:n.922-61C>T
NM_000787.4:c.922-61C>T MANE Select NP_000778.3:n.922-61C>T
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