Canonical Allele Identifier: CA1693537906
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1583467560
gnomAD v4: 7-21543244-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543244C>G , CM000669.2:g.21543244C>G GRCh38
NC_000007.13:g.21582862C>G , CM000669.1:g.21582862C>G GRCh37
NC_000007.12:g.21549387C>G NCBI36
NG_012886.2:g.5030C>G

Transcript Alleles

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