Canonical Allele Identifier: CA155122453
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs538252046
gnomAD v3: 7-21816999-C-T
gnomAD v4: 7-21816999-C-T
MyVariant Identifiers: chr7:g.21856617C>T (hg19) chr7:g.21816999C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816999C>T , CM000669.2:g.21816999C>T GRCh38
NC_000007.13:g.21856617C>T , CM000669.1:g.21856617C>T GRCh37
NC_000007.12:g.21823142C>T NCBI36
NG_012886.2:g.278785C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10568+297C>T MANE Select ENSP00000475939.1:n.10568+297C>T
ENST00000328843.10:c.10589+297C>T ENSP00000330671.7:n.10589+297C>T
ENST00000409508.7:c.10568+297C>T ENSP00000475939.1:n.10568+297C>T
ENST00000620169.4:c.10589+297C>T ENSP00000481693.1:n.10589+297C>T
NM_001277115.1:c.10568+297C>T NP_001264044.1:n.10568+297C>T
NM_001277115.2:c.10568+297C>T MANE Select NP_001264044.1:n.10568+297C>T
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