Canonical Allele Identifier: CA350493338
Gene: XRCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.216986842T>A (hg19) chr2:g.216122119T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122119T>A , CM000664.2:g.216122119T>A GRCh38
NC_000002.11:g.216986842T>A , CM000664.1:g.216986842T>A GRCh37
NC_000002.10:g.216695087T>A NCBI36
NG_029780.1:g.17823T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.549T>A MANE Select ENSP00000375977.2:p.Phe183Leu
ENST00000392132.6:c.549T>A ENSP00000375977.2:p.Phe183Leu
ENST00000392133.7:c.549T>A ENSP00000375978.3:p.Phe183Leu
ENST00000460284.5:n.1091T>A
NM_021141.3:c.549T>A NP_066964.1:p.Phe183Leu
NM_021141.4:c.549T>A MANE Select NP_066964.1:p.Phe183Leu
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