Canonical Allele Identifier: CA343643604
Gene: RNASEL HGNC NCBI

Linked Data

dbSNP Id: rs1189617674

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586028T>C , CM000663.2:g.182586028T>C GRCh38
NC_000001.10:g.182555163T>C , CM000663.1:g.182555163T>C GRCh37
NC_000001.9:g.180821786T>C NCBI36
NG_009024.2:g.5946A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.779A>G MANE Select ENSP00000356530.3:p.Glu260Gly
ENST00000539397.1:c.779A>G ENSP00000440844.1:p.Glu260Gly
NM_021133.3:c.779A>G NP_066956.1:p.Glu260Gly
XM_005245411.2:c.779A>G XP_005245468.1:p.Glu260Gly
XR_001737359.1:n.1062A>G
XR_001737360.1:n.1062A>G
NM_021133.4:c.779A>G MANE Select NP_066956.1:p.Glu260Gly