Canonical Allele Identifier: CA1211556489
Gene: RNASEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586237C= , CM000663.2:g.182586237C= GRCh38
NC_000001.10:g.182555372C= , CM000663.1:g.182555372C= GRCh37
NC_000001.9:g.180821995C= NCBI36
NG_009024.2:g.5737G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.570G= MANE Select ENSP00000356530.3:p.Glu190=
ENST00000539397.1:c.570G= ENSP00000440844.1:p.Glu190=
NM_021133.3:c.570G= NP_066956.1:p.Glu190=
XM_005245411.2:c.570G= XP_005245468.1:p.Glu190=
XR_001737359.1:n.853G=
XR_001737360.1:n.853G=
NM_021133.4:c.570G= MANE Select NP_066956.1:p.Glu190=