Canonical Allele Identifier: CA366936927
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21744082A>G (hg19) chr7:g.21704464A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21704464A>G , CM000669.2:g.21704464A>G GRCh38
NC_000007.13:g.21744082A>G , CM000669.1:g.21744082A>G GRCh37
NC_000007.12:g.21710607A>G NCBI36
NG_012886.2:g.166250A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.6304A>G MANE Select ENSP00000475939.1:p.Met2102Val
ENST00000328843.10:c.6325A>G ENSP00000330671.7:p.Met2109Val
ENST00000409508.7:c.6304A>G ENSP00000475939.1:p.Met2102Val
ENST00000620169.4:c.6325A>G ENSP00000481693.1:p.Met2109Val
NM_001277115.1:c.6304A>G NP_001264044.1:p.Met2102Val
NM_001277115.2:c.6304A>G MANE Select NP_001264044.1:p.Met2102Val
Search 100 bp 5'
Search 100 bp 3'