Canonical Allele Identifier: CA16506291
Gene: LINC02490 HGNC NCBI

Linked Data

dbSNP Id: rs719714
gnomAD v2: 15-53279378-A-G
gnomAD v3: 15-52987181-A-G
gnomAD v4: 15-52987181-A-G
MyVariant Identifiers: chr15:g.53279378A>G (hg19) chr15:g.52987181A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.52987181A>G , CM000677.2:g.52987181A>G GRCh38
NC_000015.9:g.53279378A>G , CM000677.1:g.53279378A>G GRCh37
NC_000015.8:g.51066670A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932256.1:n.463+11332A>G
XR_932257.1:n.463+11332A>G
XM_017022782.1:c.*4896A>G XP_016878271.1:n.*4896A>G
XM_017022783.1:c.*4896A>G XP_016878272.1:n.*4896A>G
XM_017022784.1:c.451+11332A>G XP_016878273.1:n.451+11332A>G
XM_017022785.1:c.451+11332A>G XP_016878274.1:n.451+11332A>G
XR_001751547.1:n.5434A>G
XR_001751548.1:n.552+11332A>G
XR_932257.2:n.533+11332A>G
XR_004837528.1:n.5584A>G
XR_004837529.1:n.5519A>G
XR_004837530.1:n.533+11332A>G
XR_004837531.1:n.533+11332A>G
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