Canonical Allele Identifier: CA13634622
Gene: KSR2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10444502

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117916066A>C , CM000674.2:g.117916066A>C GRCh38
NC_000012.11:g.118353871A>C , CM000674.1:g.118353871A>C GRCh37
NC_000012.10:g.116838254A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_173598.4:c.93+52010T>G VV NP_775869.3:p.=
XM_011538224.1:c.180+52010T>G XP_011536526.1:p.=
XM_011538226.1:c.180+52010T>G XP_011536528.1:p.=
XM_011538229.1:c.180+52010T>G XP_011536531.1:p.=
XR_944522.1:n.1014+52010T>G
XM_011538224.3:c.180+52010T>G
XM_011538226.3:c.180+52010T>G
XM_011538229.3:c.180+52010T>G
XM_017019208.2:c.180+52010T>G XP_016874697.1:p.=
XM_017019209.2:c.180+52010T>G XP_016874698.1:p.=
ENST00000339824.6:c.180+52010T>G ENSP00000339952.4:p.=
ENST00000425217.5:c.93+52010T>G ENSP00000389715.1:p.=