Canonical Allele Identifier: CA1693626790
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1295891041
gnomAD v4: 7-21705578-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705578C>A , CM000669.2:g.21705578C>A GRCh38
NC_000007.13:g.21745196C>A , CM000669.1:g.21745196C>A GRCh37
NC_000007.12:g.21711721C>A NCBI36
NG_012886.2:g.167364C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6546+41C>A MANE Select ENSP00000475939.1:n.6546+41C>A
ENST00000328843.10:c.6567+41C>A ENSP00000330671.7:n.6567+41C>A
ENST00000409508.7:c.6546+41C>A ENSP00000475939.1:n.6546+41C>A
ENST00000620169.4:c.6567+41C>A ENSP00000481693.1:n.6567+41C>A
NM_001277115.1:c.6546+41C>A NP_001264044.1:n.6546+41C>A
NM_001277115.2:c.6546+41C>A MANE Select NP_001264044.1:n.6546+41C>A
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