Canonical Allele Identifier: CA885992991

Gene: CD58

Linked Data

• dbSNP Id: rs1306083674
• MyVariant Identifiers: chr1:g.117087733A>G (hg19) ; chr1:g.116545111A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545111A>G , CM000663.2:g.116545111A>G	GRCh38
NC_000001.10:g.117087733A>G , CM000663.1:g.117087733A>G	GRCh37
NC_000001.9:g.116889256A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.71-507T>C MANE Select	ENSP00000358501.5:n.71-507T>C
ENST00000369487.3:c.71-507T>C	ENSP00000358499.3:n.71-507T>C
ENST00000369489.9:c.71-507T>C	ENSP00000358501.5:n.71-507T>C
ENST00000457047.6:c.71-507T>C	ENSP00000409080.2:n.71-507T>C
ENST00000464088.5:c.71-507T>C	ENSP00000432773.1:n.71-507T>C
NM_001144822.1:c.71-507T>C	NP_001138294.1:n.71-507T>C
NM_001779.2:c.71-507T>C	NP_001770.1:n.71-507T>C
NR_026665.1:n.192-507T>C
XR_947739.1:n.210+287A>G
XR_947740.1:n.210+287A>G
XM_017002869.2:c.71-507T>C	XP_016858358.1:n.71-507T>C
NM_001779.3:c.71-507T>C MANE Select	NP_001770.1:n.71-507T>C
NR_026665.2:n.125-507T>C
NM_001144822.2:c.71-507T>C	NP_001138294.1:n.71-507T>C