Canonical Allele Identifier: CA343643832
Gene: RNASEL HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.182555242C>A (hg19) chr1:g.182586107C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586107C>A , CM000663.2:g.182586107C>A GRCh38
NC_000001.10:g.182555242C>A , CM000663.1:g.182555242C>A GRCh37
NC_000001.9:g.180821865C>A NCBI36
NG_009024.2:g.5867G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.700G>T MANE Select ENSP00000356530.3:p.Val234Leu
ENST00000539397.1:c.700G>T ENSP00000440844.1:p.Val234Leu
NM_021133.3:c.700G>T NP_066956.1:p.Val234Leu
XM_005245411.2:c.700G>T XP_005245468.1:p.Val234Leu
XR_001737359.1:n.983G>T
XR_001737360.1:n.983G>T
NM_021133.4:c.700G>T MANE Select NP_066956.1:p.Val234Leu
Search 100 bp 5'
Search 100 bp 3'