Canonical Allele Identifier: CA265952604
Gene: CLMN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs115102486

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95298227A>G , CM000676.2:g.95298227A>G GRCh38
NC_000014.8:g.95764564A>G , CM000676.1:g.95764564A>G GRCh37
NC_000014.7:g.94834317A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_024734.3:c.82+21484T>C VV NP_079010.2:p.=
XM_011537158.1:c.82+21484T>C XP_011535460.1:p.=
XM_011537159.1:c.82+21484T>C XP_011535461.1:p.=
XR_245721.2:n.194+21484T>C
XR_429330.2:n.194+21484T>C
XR_429332.2:n.194+21484T>C
XM_011537159.2:c.82+21484T>C
XM_017021646.1:c.22+21012T>C XP_016877135.1:p.=
XM_017021647.1:c.82+21484T>C XP_016877136.1:p.=
XR_001750558.1:n.194+21484T>C
NM_024734.4:c.82+21484T>C VV MANE Preferred
ENST00000298912.8:c.82+21484T>C ENSP00000298912.3:p.=
ENST00000553733.1:c.82+21484T>C ENSP00000451189.1:p.=
ENST00000555615.1:c.-123+9287T>C ENSP00000452525.1:p.=