Canonical Allele Identifier: CA366963991
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 971122
ClinVar RCV Id: RCV001246823
dbSNP Id: rs1229709690
gnomAD v2: 7-21920386-C-T
gnomAD v4: 7-21880768-C-T
MyVariant Identifiers: chr7:g.21920386C>T (hg19) chr7:g.21880768C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880768C>T , CM000669.2:g.21880768C>T GRCh38
NC_000007.13:g.21920386C>T , CM000669.1:g.21920386C>T GRCh37
NC_000007.12:g.21886911C>T NCBI36
NG_012886.2:g.342554C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.12262C>T MANE Select ENSP00000475939.1:p.His4088Tyr
ENST00000328843.10:c.12283C>T ENSP00000330671.7:p.His4095Tyr
ENST00000409508.7:c.12262C>T ENSP00000475939.1:p.His4088Tyr
ENST00000620169.4:c.12283C>T ENSP00000481693.1:p.His4095Tyr
NM_001277115.1:c.12262C>T NP_001264044.1:p.His4088Tyr
NM_001277115.2:c.12262C>T MANE Select NP_001264044.1:p.His4088Tyr
Search 100 bp 5'
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