Canonical Allele Identifier: CA113752061
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs12518614
gnomAD v2: 5-6324293-A-G
gnomAD v3: 5-6324180-A-G
gnomAD v4: 5-6324180-A-G
MyVariant Identifiers: chr5:g.6324293A>G (hg19) chr5:g.6324180A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324180A>G , CM000667.2:g.6324180A>G GRCh38
NC_000005.9:g.6324293A>G , CM000667.1:g.6324293A>G GRCh37
NC_000005.8:g.6377293A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028351.1:n.144-11464T>C
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