Canonical Allele Identifier: CA453963489
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21599957-A-G
MyVariant Identifiers: chr7:g.21639575A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599957A>G , CM000669.2:g.21599957A>G GRCh38
NC_000007.13:g.21639575A>G , CM000669.1:g.21639575A>G GRCh37
NC_000007.12:g.21606100A>G NCBI36
NG_012886.2:g.61743A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.2838A>G MANE Select ENSP00000475939.1:p.Ala946=
ENST00000328843.10:c.2838A>G ENSP00000330671.7:p.Ala946=
ENST00000409508.7:c.2838A>G ENSP00000475939.1:p.Ala946=
ENST00000620169.4:c.2838A>G ENSP00000481693.1:p.Ala946=
NM_001277115.1:c.2838A>G NP_001264044.1:p.Ala946=
NM_001277115.2:c.2838A>G MANE Select NP_001264044.1:p.Ala946=
Search 100 bp 5'
Search 100 bp 3'