Canonical Allele Identifier: CA14489100
Gene: DNAH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16956936

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7730374C>T , CM000679.2:g.7730374C>T GRCh38
NC_000017.9:g.7574417C>T NCBI36
NC_000017.10:g.7633692C>T , CM000679.1:g.7633692C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000389173.6:c.400-2713C>T ENSP00000373825.2:p.=
ENST00000570791.5:c.400-2713C>T ENSP00000460245.1:p.=
ENST00000572933.5:c.400-2713C>T ENSP00000458355.1:p.=
NM_001303270.1:c.400-2713C>T VV NP_001290199.1:p.=
NM_020877.3:c.400-2713C>T VV NP_065928.2:p.=
XM_011523663.1:c.400-2713C>T XP_011521965.1:p.=
XM_011523664.1:c.400-2713C>T XP_011521966.1:p.=
XM_011523665.1:c.400-2713C>T XP_011521967.1:p.=
XM_011523666.1:c.400-2713C>T XP_011521968.1:p.=
XM_011523667.1:c.400-2713C>T XP_011521969.1:p.=
XM_011523670.1:c.400-2713C>T XP_011521972.1:p.=
XM_011523667.2:c.400-2713C>T
XM_011523670.2:c.400-2713C>T
XM_017024219.1:c.400-2713C>T XP_016879708.1:p.=
XM_024450604.1:c.400-2713C>T XP_024306372.1:p.=
XM_024450605.1:c.400-2713C>T XP_024306373.1:p.=
XM_024450606.1:c.400-2713C>T XP_024306374.1:p.=
XM_024450607.1:c.400-2713C>T XP_024306375.1:p.=