Canonical Allele Identifier: CA366948508
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21856188C>T (hg19) chr7:g.21816570C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816570C>T , CM000669.2:g.21816570C>T GRCh38
NC_000007.13:g.21856188C>T , CM000669.1:g.21856188C>T GRCh37
NC_000007.12:g.21822713C>T NCBI36
NG_012886.2:g.278356C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10436C>T MANE Select ENSP00000475939.1:p.Ser3479Phe
ENST00000328843.10:c.10457C>T ENSP00000330671.7:p.Ser3486Phe
ENST00000409508.7:c.10436C>T ENSP00000475939.1:p.Ser3479Phe
ENST00000620169.4:c.10457C>T ENSP00000481693.1:p.Ser3486Phe
NM_001277115.1:c.10436C>T NP_001264044.1:p.Ser3479Phe
NM_001277115.2:c.10436C>T MANE Select NP_001264044.1:p.Ser3479Phe
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