Canonical Allele Identifier: CA169486919
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1054474643
gnomAD v4: 7-152648448-C-A
MyVariant Identifiers: chr7:g.152345533C>A (hg19) chr7:g.152648448C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648448C>A , CM000669.2:g.152648448C>A GRCh38
NC_000007.13:g.152345533C>A , CM000669.1:g.152345533C>A GRCh37
NC_000007.12:g.151976466C>A NCBI36
NG_027988.1:g.32718G>T
NG_027988.2:g.32718G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*194G>T ENSP00000513758.1:n.*194G>T
ENST00000359321.2:c.*194G>T MANE Select ENSP00000352271.1:n.*194G>T
ENST00000359321.1:c.*194G>T ENSP00000352271.1:n.*194G>T
ENST00000495707.1:n.1059G>T
NM_005431.1:c.*194G>T NP_005422.1:n.*194G>T
NM_005431.2:c.*194G>T MANE Select NP_005422.1:n.*194G>T
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