Canonical Allele Identifier: CA155087057
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs752195932
gnomAD v4: 7-21599895-G-T
MyVariant Identifiers: chr7:g.21639513G>T (hg19) chr7:g.21599895G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599895G>T , CM000669.2:g.21599895G>T GRCh38
NC_000007.13:g.21639513G>T , CM000669.1:g.21639513G>T GRCh37
NC_000007.12:g.21606038G>T NCBI36
NG_012886.2:g.61681G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2776G>T MANE Select ENSP00000475939.1:p.Asp926Tyr
ENST00000328843.10:c.2776G>T ENSP00000330671.7:p.Asp926Tyr
ENST00000409508.7:c.2776G>T ENSP00000475939.1:p.Asp926Tyr
ENST00000620169.4:c.2776G>T ENSP00000481693.1:p.Asp926Tyr
NM_001277115.1:c.2776G>T NP_001264044.1:p.Asp926Tyr
NM_001277115.2:c.2776G>T MANE Select NP_001264044.1:p.Asp926Tyr
Search 100 bp 5'
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