Canonical Allele Identifier: CA37393246
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs572424933
gnomAD v3: 1-214087797-C-T
gnomAD v4: 1-214087797-C-T
MyVariant Identifiers: chr1:g.214261140C>T (hg19) chr1:g.214087797C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087797C>T , CM000663.2:g.214087797C>T GRCh38
NC_000001.10:g.214261140C>T , CM000663.1:g.214261140C>T GRCh37
NC_000001.9:g.212327763C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15359G>A XP_011508605.1:n.-188-15359G>A
XR_922584.1:n.119-15359G>A
XR_922584.2:n.261-15359G>A
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