Canonical Allele Identifier: CA1211556516
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586320G= , CM000663.2:g.182586320G= GRCh38
NC_000001.10:g.182555455G= , CM000663.1:g.182555455G= GRCh37
NC_000001.9:g.180822078G= NCBI36
NG_009024.2:g.5654C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.487C= MANE Select ENSP00000356530.3:p.Arg163=
ENST00000539397.1:c.487C= ENSP00000440844.1:p.Arg163=
NM_021133.3:c.487C= NP_066956.1:p.Arg163=
XM_005245411.2:c.487C= XP_005245468.1:p.Arg163=
XR_001737359.1:n.770C=
XR_001737360.1:n.770C=
NM_021133.4:c.487C= MANE Select NP_066956.1:p.Arg163=