Canonical Allele Identifier: CA343644074
Gene: RNASEL HGNC NCBI

Linked Data

gnomAD v4: 1-182586161-T-G
MyVariant Identifiers: chr1:g.182555296T>G (hg19) chr1:g.182586161T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586161T>G , CM000663.2:g.182586161T>G GRCh38
NC_000001.10:g.182555296T>G , CM000663.1:g.182555296T>G GRCh37
NC_000001.9:g.180821919T>G NCBI36
NG_009024.2:g.5813A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.646A>C MANE Select ENSP00000356530.3:p.Ser216Arg
ENST00000539397.1:c.646A>C ENSP00000440844.1:p.Ser216Arg
NM_021133.3:c.646A>C NP_066956.1:p.Ser216Arg
XM_005245411.2:c.646A>C XP_005245468.1:p.Ser216Arg
XR_001737359.1:n.929A>C
XR_001737360.1:n.929A>C
NM_021133.4:c.646A>C MANE Select NP_066956.1:p.Ser216Arg
Search 100 bp 5'
Search 100 bp 3'