Canonical Allele Identifier: CA1129759557
Gene: DBH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644180_133644181insTTTTTTAAT , CM000671.2:g.133644180_133644181insTTTTTTAAT GRCh38
NC_000009.11:g.136509302_136509303insTTTTTTAAT , CM000671.1:g.136509302_136509303insTTTTTTAAT GRCh37
NC_000009.10:g.135499123_135499124insTTTTTTAAT NCBI36
NG_008645.1:g.12818_12819insTTTTTTAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-38_922-37insTTTTTTAAT MANE Select ENSP00000376776.2:n.922-38_922-37insTTTTTTAAT
ENST00000393056.6:c.922-38_922-37insTTTTTTAAT ENSP00000376776.2:n.922-38_922-37insTTTTTTAAT
NM_000787.3:c.922-38_922-37insTTTTTTAAT NP_000778.3:n.922-38_922-37insTTTTTTAAT
NM_000787.4:c.922-38_922-37insTTTTTTAAT MANE Select NP_000778.3:n.922-38_922-37insTTTTTTAAT