Canonical Allele Identifier: CA4178728
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3221490
ClinVar RCV Id: RCV004508341
dbSNP Id: rs753456838
ExAC: 7:21598561 C / T
gnomAD v2: 7-21598561-C-T
gnomAD v3: 7-21558943-C-T
gnomAD v4: 7-21558943-C-T
MyVariant Identifiers: chr7:g.21598561C>T (hg19) chr7:g.21558943C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558943C>T , CM000669.2:g.21558943C>T GRCh38
NC_000007.13:g.21598561C>T , CM000669.1:g.21598561C>T GRCh37
NC_000007.12:g.21565086C>T NCBI36
NG_012886.2:g.20729C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.637C>T MANE Select ENSP00000475939.1:p.Pro213Ser
ENST00000328843.10:c.637C>T ENSP00000330671.7:p.Pro213Ser
ENST00000409508.7:c.637C>T ENSP00000475939.1:p.Pro213Ser
ENST00000620169.4:c.637C>T ENSP00000481693.1:p.Pro213Ser
NM_001277115.1:c.637C>T NP_001264044.1:p.Pro213Ser
NM_001277115.2:c.637C>T MANE Select NP_001264044.1:p.Pro213Ser
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