Canonical Allele Identifier: CA1099223921
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs772166460
gnomAD v3: 7-21558559-T-A
gnomAD v4: 7-21558559-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558559T>A , CM000669.2:g.21558559T>A GRCh38
NC_000007.13:g.21598177T>A , CM000669.1:g.21598177T>A GRCh37
NC_000007.12:g.21564702T>A NCBI36
NG_012886.2:g.20345T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.496-243T>A MANE Select ENSP00000475939.1:n.496-243T>A
ENST00000328843.10:c.496-243T>A ENSP00000330671.7:n.496-243T>A
ENST00000409508.7:c.496-243T>A ENSP00000475939.1:n.496-243T>A
ENST00000620169.4:c.496-243T>A ENSP00000481693.1:n.496-243T>A
NM_001277115.1:c.496-243T>A NP_001264044.1:n.496-243T>A
NM_001277115.2:c.496-243T>A MANE Select NP_001264044.1:n.496-243T>A
Search 100 bp 5'
Search 100 bp 3'