Canonical Allele Identifier: CA350493533
Gene: XRCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.216986929G>T (hg19) chr2:g.216122206G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122206G>T , CM000664.2:g.216122206G>T GRCh38
NC_000002.11:g.216986929G>T , CM000664.1:g.216986929G>T GRCh37
NC_000002.10:g.216695174G>T NCBI36
NG_029780.1:g.17910G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392132.7:c.636G>T MANE Select ENSP00000375977.2:p.Met212Ile
ENST00000392132.6:c.636G>T ENSP00000375977.2:p.Met212Ile
ENST00000392133.7:c.636G>T ENSP00000375978.3:p.Met212Ile
ENST00000460284.5:n.1178G>T
NM_021141.3:c.636G>T NP_066964.1:p.Met212Ile
NM_021141.4:c.636G>T MANE Select NP_066964.1:p.Met212Ile
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