Canonical Allele Identifier: CA4582272
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs547985094
ExAC: 7:152345703 C / T
gnomAD v2: 7-152345703-C-T
gnomAD v3: 7-152648618-C-T
gnomAD v4: 7-152648618-C-T
MyVariant Identifiers: chr7:g.152345703C>T (hg19) chr7:g.152345703_152345705delinsTAA (hg19) chr7:g.152648618C>T (hg38) chr7:g.152648618_152648620delinsTAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648618C>T , CM000669.2:g.152648618C>T GRCh38
NC_000007.13:g.152345703C>T , CM000669.1:g.152345703C>T GRCh37
NC_000007.12:g.151976636C>T NCBI36
NG_027988.1:g.32548G>A
NG_027988.2:g.32548G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*24G>A ENSP00000513758.1:n.*24G>A
ENST00000359321.2:c.*24G>A MANE Select ENSP00000352271.1:n.*24G>A
ENST00000359321.1:c.*24G>A ENSP00000352271.1:n.*24G>A
ENST00000495707.1:n.889G>A
NM_005431.1:c.*24G>A NP_005422.1:n.*24G>A
NM_005431.2:c.*24G>A MANE Select NP_005422.1:n.*24G>A
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