Canonical Allele Identifier: CA29684771

Gene: CD58

Linked Data

• dbSNP Id: rs1022236221
• gnomAD v3: 1-116544999-A-G
• gnomAD v4: 1-116544999-A-G
• MyVariant Identifiers: chr1:g.117087621A>G (hg19) ; chr1:g.116544999A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116544999A>G , CM000663.2:g.116544999A>G	GRCh38
NC_000001.10:g.117087621A>G , CM000663.1:g.117087621A>G	GRCh37
NC_000001.9:g.116889144A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369489.10:c.71-395T>C MANE Select	ENSP00000358501.5:n.71-395T>C
ENST00000369487.3:c.71-395T>C	ENSP00000358499.3:n.71-395T>C
ENST00000369489.9:c.71-395T>C	ENSP00000358501.5:n.71-395T>C
ENST00000457047.6:c.71-395T>C	ENSP00000409080.2:n.71-395T>C
ENST00000464088.5:c.71-395T>C	ENSP00000432773.1:n.71-395T>C
NM_001144822.1:c.71-395T>C	NP_001138294.1:n.71-395T>C
NM_001779.2:c.71-395T>C	NP_001770.1:n.71-395T>C
NR_026665.1:n.192-395T>C
XR_947739.1:n.210+175A>G
XR_947740.1:n.210+175A>G
XM_017002869.2:c.71-395T>C	XP_016858358.1:n.71-395T>C
NM_001779.3:c.71-395T>C MANE Select	NP_001770.1:n.71-395T>C
NR_026665.2:n.125-395T>C
NM_001144822.2:c.71-395T>C	NP_001138294.1:n.71-395T>C