Canonical Allele Identifier: CA1211556496
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586266C= , CM000663.2:g.182586266C= GRCh38
NC_000001.10:g.182555401C= , CM000663.1:g.182555401C= GRCh37
NC_000001.9:g.180822024C= NCBI36
NG_009024.2:g.5708G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.541G= MANE Select ENSP00000356530.3:p.Val181=
ENST00000539397.1:c.541G= ENSP00000440844.1:p.Val181=
NM_021133.3:c.541G= NP_066956.1:p.Val181=
XM_005245411.2:c.541G= XP_005245468.1:p.Val181=
XR_001737359.1:n.824G=
XR_001737360.1:n.824G=
NM_021133.4:c.541G= MANE Select NP_066956.1:p.Val181=