Canonical Allele Identifier: CA343644913
Gene: RNASEL HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.182555486A>C (hg19) chr1:g.182586351A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586351A>C , CM000663.2:g.182586351A>C GRCh38
NC_000001.10:g.182555486A>C , CM000663.1:g.182555486A>C GRCh37
NC_000001.9:g.180822109A>C NCBI36
NG_009024.2:g.5623T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.456T>G MANE Select ENSP00000356530.3:p.Asn152Lys
ENST00000539397.1:c.456T>G ENSP00000440844.1:p.Asn152Lys
NM_021133.3:c.456T>G NP_066956.1:p.Asn152Lys
XM_005245411.2:c.456T>G XP_005245468.1:p.Asn152Lys
XR_001737359.1:n.739T>G
XR_001737360.1:n.739T>G
NM_021133.4:c.456T>G MANE Select NP_066956.1:p.Asn152Lys
Search 100 bp 5'
Search 100 bp 3'