Canonical Allele Identifier: CA1230881
Gene: XCL2 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.168540975T>A
GRCh37 chr1:g.168510213T>A
Revel Score:
ENST00000367819 (MANE Select) 0.059
gnomAD v2:
1:168510213 T / A
gnomAD v3:
1:168540975 T / A
gnomAD v4:
chr1-168540975-T-A
Joint Max Group AF 0.00037042 (NFE)
Genomes Max Group AF 0.00032956 (NFE)
Exomes Max Group AF 0.00036672 (NFE)
ClinVar RCV:
RCV004207140
ClinVar Variation:
2367690
dbSNP:
148500645
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168540975T>A , CM000663.2:g.168540975T>A GRCh38
NC_000001.10:g.168510213T>A , CM000663.1:g.168510213T>A GRCh37
NC_000001.9:g.166776837T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367819.3:c.322A>T MANE Select ENSP00000356793.2:p.Thr108Ser
ENST00000367819.2:c.322A>T ENSP00000356793.2:p.Thr108Ser
NM_003175.3:c.322A>T NP_003166.1:p.Thr108Ser
NM_003175.4:c.322A>T MANE Select NP_003166.1:p.Thr108Ser
Search 100 bp 5'
Search 100 bp 3'