Canonical Allele Identifier: CA29684819

Gene: CD58

Linked Data

• dbSNP Id: rs1018563796
• gnomAD v3: 1-116545060-G-T
• gnomAD v4: 1-116545060-G-T
• MyVariant Identifiers: chr1:g.117087682G>T (hg19) ; chr1:g.116545060G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116545060G>T , CM000663.2:g.116545060G>T	GRCh38
NC_000001.10:g.117087682G>T , CM000663.1:g.117087682G>T	GRCh37
NC_000001.9:g.116889205G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369489.10:c.71-456C>A MANE Select	ENSP00000358501.5:n.71-456C>A
ENST00000369487.3:c.71-456C>A	ENSP00000358499.3:n.71-456C>A
ENST00000369489.9:c.71-456C>A	ENSP00000358501.5:n.71-456C>A
ENST00000457047.6:c.71-456C>A	ENSP00000409080.2:n.71-456C>A
ENST00000464088.5:c.71-456C>A	ENSP00000432773.1:n.71-456C>A
NM_001144822.1:c.71-456C>A	NP_001138294.1:n.71-456C>A
NM_001779.2:c.71-456C>A	NP_001770.1:n.71-456C>A
NR_026665.1:n.192-456C>A
XR_947739.1:n.210+236G>T
XR_947740.1:n.210+236G>T
XM_017002869.2:c.71-456C>A	XP_016858358.1:n.71-456C>A
NM_001779.3:c.71-456C>A MANE Select	NP_001770.1:n.71-456C>A
NR_026665.2:n.125-456C>A
NM_001144822.2:c.71-456C>A	NP_001138294.1:n.71-456C>A