Canonical Allele Identifier: CA1211556449
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586112A= , CM000663.2:g.182586112A= GRCh38
NC_000001.10:g.182555247A= , CM000663.1:g.182555247A= GRCh37
NC_000001.9:g.180821870A= NCBI36
NG_009024.2:g.5862T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.695T= MANE Select ENSP00000356530.3:p.Val232=
ENST00000539397.1:c.695T= ENSP00000440844.1:p.Val232=
NM_021133.3:c.695T= NP_066956.1:p.Val232=
XM_005245411.2:c.695T= XP_005245468.1:p.Val232=
XR_001737359.1:n.978T=
XR_001737360.1:n.978T=
NM_021133.4:c.695T= MANE Select NP_066956.1:p.Val232=