Canonical Allele Identifier: CA366955117
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039760
ClinVar RCV Id: RCV001343302
dbSNP Id: rs1363623324
MyVariant Identifiers: chr7:g.21788241C>G (hg19) chr7:g.21748623C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748623C>G , CM000669.2:g.21748623C>G GRCh38
NC_000007.13:g.21788241C>G , CM000669.1:g.21788241C>G GRCh37
NC_000007.12:g.21754766C>G NCBI36
NG_012886.2:g.210409C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8554C>G MANE Select ENSP00000475939.1:p.Leu2852Val
ENST00000328843.10:c.8575C>G ENSP00000330671.7:p.Leu2859Val
ENST00000409508.7:c.8554C>G ENSP00000475939.1:p.Leu2852Val
ENST00000620169.4:c.8575C>G ENSP00000481693.1:p.Leu2859Val
NM_001277115.1:c.8554C>G NP_001264044.1:p.Leu2852Val
NM_001277115.2:c.8554C>G MANE Select NP_001264044.1:p.Leu2852Val
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