Canonical Allele Identifier: CA1525089319
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs781076540
gnomAD v3: 5-6324201-G-A
gnomAD v4: 5-6324201-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324201G>A , CM000667.2:g.6324201G>A GRCh38
NC_000005.9:g.6324314G>A , CM000667.1:g.6324314G>A GRCh37
NC_000005.8:g.6377314G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028351.1:n.144-11485C>T
Search 100 bp 5'
Search 100 bp 3'