Canonical Allele Identifier: CA1619098589
Gene: LINC02571 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306528_31306533delinsCTCTTT , CM000668.2:g.31306528_31306533delinsCTCTTT GRCh38
NC_000006.11:g.31274305_31274310delinsCTCTTT , CM000668.1:g.31274305_31274310delinsCTCTTT GRCh37
NC_000006.10:g.31382284_31382289delinsCTCTTT NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+245_949+250delinsAAAGAG
XR_926691.2:n.965+245_965+250delinsAAAGAG