Canonical Allele Identifier: CA324608698
Gene: XRCC6 HGNC NCBI

Linked Data

dbSNP Id: rs1043467338
gnomAD v4: 22-41621224-T-A
MyVariant Identifiers: chr22:g.41621224T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621224T>A , CM000684.2:g.41621224T>A GRCh38
NC_000022.10:g.42017228T>A , CM000684.1:g.42017228T>A GRCh37
NC_000022.9:g.40347174T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.7:c.-137T>A ENSP00000353192.3:n.-137T>A
ENST00000428575.6:c.-174T>A ENSP00000403679.3:n.-174T>A
NM_001288977.1:c.-137T>A NP_001275906.1:n.-137T>A
NM_001288978.1:c.-174T>A NP_001275907.1:n.-174T>A
NM_001469.4:c.-137T>A NP_001460.1:n.-137T>A
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