Canonical Allele Identifier: CA1211556498
Gene: RNASEL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586271C= , CM000663.2:g.182586271C= GRCh38
NC_000001.10:g.182555406C= , CM000663.1:g.182555406C= GRCh37
NC_000001.9:g.180822029C= NCBI36
NG_009024.2:g.5703G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.536G= MANE Select ENSP00000356530.3:p.Gly179=
ENST00000539397.1:c.536G= ENSP00000440844.1:p.Gly179=
NM_021133.3:c.536G= NP_066956.1:p.Gly179=
XM_005245411.2:c.536G= XP_005245468.1:p.Gly179=
XR_001737359.1:n.819G=
XR_001737360.1:n.819G=
NM_021133.4:c.536G= MANE Select NP_066956.1:p.Gly179=
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