Canonical Allele Identifier: CA528919737
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1238105113
gnomAD v2: 1-214261075-T-C
gnomAD v3: 1-214087732-T-C
gnomAD v4: 1-214087732-T-C
MyVariant Identifiers: chr1:g.214261075T>C (hg19) chr1:g.214087732T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087732T>C , CM000663.2:g.214087732T>C GRCh38
NC_000001.10:g.214261075T>C , CM000663.1:g.214261075T>C GRCh37
NC_000001.9:g.212327698T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15294A>G XP_011508605.1:n.-188-15294A>G
XR_922584.1:n.119-15294A>G
XR_922584.2:n.261-15294A>G
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