Canonical Allele Identifier: CA573292954
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1310256394
gnomAD v2: 7-21920309-T-C
gnomAD v4: 7-21880691-T-C
MyVariant Identifiers: chr7:g.21920309T>C (hg19) chr7:g.21880691T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880691T>C , CM000669.2:g.21880691T>C GRCh38
NC_000007.13:g.21920309T>C , CM000669.1:g.21920309T>C GRCh37
NC_000007.12:g.21886834T>C NCBI36
NG_012886.2:g.342477T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.12196-11T>C MANE Select ENSP00000475939.1:n.12196-11T>C
ENST00000328843.10:c.12217-11T>C ENSP00000330671.7:n.12217-11T>C
ENST00000409508.7:c.12196-11T>C ENSP00000475939.1:n.12196-11T>C
ENST00000620169.4:c.12217-11T>C ENSP00000481693.1:n.12217-11T>C
NM_001277115.1:c.12196-11T>C NP_001264044.1:n.12196-11T>C
NM_001277115.2:c.12196-11T>C MANE Select NP_001264044.1:n.12196-11T>C
Search 100 bp 5'
Search 100 bp 3'