Canonical Allele Identifier: CA343644631
Gene: RNASEL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586281C>G , CM000663.2:g.182586281C>G GRCh38
NC_000001.10:g.182555416C>G , CM000663.1:g.182555416C>G GRCh37
NC_000001.9:g.180822039C>G NCBI36
NG_009024.2:g.5693G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.526G>C MANE Select ENSP00000356530.3:p.Ala176Pro
ENST00000539397.1:c.526G>C ENSP00000440844.1:p.Ala176Pro
NM_021133.3:c.526G>C NP_066956.1:p.Ala176Pro
XM_005245411.2:c.526G>C XP_005245468.1:p.Ala176Pro
XR_001737359.1:n.809G>C
XR_001737360.1:n.809G>C
NM_021133.4:c.526G>C MANE Select NP_066956.1:p.Ala176Pro