Canonical Allele Identifier: CA350493336
Gene: XRCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.216986841T>C (hg19) chr2:g.216122118T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122118T>C , CM000664.2:g.216122118T>C GRCh38
NC_000002.11:g.216986841T>C , CM000664.1:g.216986841T>C GRCh37
NC_000002.10:g.216695086T>C NCBI36
NG_029780.1:g.17822T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.548T>C MANE Select ENSP00000375977.2:p.Phe183Ser
ENST00000392132.6:c.548T>C ENSP00000375977.2:p.Phe183Ser
ENST00000392133.7:c.548T>C ENSP00000375978.3:p.Phe183Ser
ENST00000460284.5:n.1090T>C
NM_021141.3:c.548T>C NP_066964.1:p.Phe183Ser
NM_021141.4:c.548T>C MANE Select NP_066964.1:p.Phe183Ser
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