Canonical Allele Identifier: CA15069358
Gene: RNASEL HGNC NCBI

Linked Data

dbSNP Id: rs3738579

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586901A>G , CM000663.2:g.182586901A>G GRCh38
NC_000001.10:g.182556036A>G , CM000663.1:g.182556036A>G GRCh37
NC_000001.9:g.180822659A>G NCBI36
NG_009024.2:g.5073T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367559.7:c.-95T>C MANE Select ENSP00000356530.3:n.-95T>C
ENST00000539397.1:c.-95T>C ENSP00000440844.1:n.-95T>C
NM_021133.3:c.-95T>C NP_066956.1:n.-95T>C
XM_005245411.2:c.-95T>C XP_005245468.1:n.-95T>C
XR_001737359.1:n.189T>C
XR_001737360.1:n.189T>C
NM_021133.4:c.-95T>C MANE Select NP_066956.1:n.-95T>C