Canonical Allele Identifier: CA1278264
Gene: RNASEL HGNC NCBI

Linked Data

dbSNP Id: rs758986186

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586274T>C , CM000663.2:g.182586274T>C GRCh38
NC_000001.10:g.182555409T>C , CM000663.1:g.182555409T>C GRCh37
NC_000001.9:g.180822032T>C NCBI36
NG_009024.2:g.5700A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.533A>G MANE Select ENSP00000356530.3:p.Lys178Arg
ENST00000539397.1:c.533A>G ENSP00000440844.1:p.Lys178Arg
NM_021133.3:c.533A>G NP_066956.1:p.Lys178Arg
XM_005245411.2:c.533A>G XP_005245468.1:p.Lys178Arg
XR_001737359.1:n.816A>G
XR_001737360.1:n.816A>G
NM_021133.4:c.533A>G MANE Select NP_066956.1:p.Lys178Arg