Canonical Allele Identifier: CA566338535
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1554193175
gnomAD v2: 6-31274518-T-TCCGGGAGTCCAGCACGTCC
gnomAD v3: 6-31306741-T-TCCGGGAGTCCAGCACGTCC
gnomAD v4: 6-31306741-T-TCCGGGAGTCCAGCACGTCC
MyVariant Identifiers: chr6:g.31274518_31274519insCCGGGAGTCCAGCACGTCC (hg19) chr6:g.31306741_31306742insCCGGGAGTCCAGCACGTCC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306755_31306756insCGTCCCCGGGAGTCCAGCA , CM000668.2:g.31306755_31306756insCGTCCCCGGGAGTCCAGCA GRCh38
NC_000006.11:g.31274532_31274533insCGTCCCCGGGAGTCCAGCA , CM000668.1:g.31274532_31274533insCGTCCCCGGGAGTCCAGCA GRCh37
NC_000006.10:g.31382511_31382512insCGTCCCCGGGAGTCCAGCA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+36_949+37insGGACGTGCTGGACTCCCGG
XR_926691.2:n.965+36_965+37insGGACGTGCTGGACTCCCGG
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