Canonical Allele Identifier: CA458803845
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152357814C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660729C>T , CM000669.2:g.152660729C>T GRCh38
NC_000007.13:g.152357814C>T , CM000669.1:g.152357814C>T GRCh37
NC_000007.12:g.151988747C>T NCBI36
NG_027988.1:g.20437G>A
NG_027988.2:g.20437G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11366G>A ENSP00000513758.1:n.-47-11366G>A
ENST00000698507.1:n.161G>A
ENST00000359321.2:c.93G>A MANE Select ENSP00000352271.1:p.Leu31=
ENST00000359321.1:c.93G>A ENSP00000352271.1:p.Leu31=
ENST00000495707.1:n.115G>A
NM_005431.1:c.93G>A NP_005422.1:p.Leu31=
NM_005431.2:c.93G>A MANE Select NP_005422.1:p.Leu31=