Canonical Allele Identifier: CA141748137
Gene: LINC02540 HGNC NCBI

Linked Data

dbSNP Id: rs12198063
gnomAD v2: 6-77290799-A-G
gnomAD v3: 6-76581082-A-G
gnomAD v4: 6-76581082-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.76581082A>G , CM000668.2:g.76581082A>G GRCh38
NC_000006.11:g.77290799A>G , CM000668.1:g.77290799A>G GRCh37
NC_000006.10:g.77347518A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942695.1:n.394-2000T>C
XR_942696.1:n.393+5366T>C
NR_149101.1:n.216+5366T>C