Canonical Allele Identifier: CA238149633
Gene: LINC01465 HGNC NCBI

Linked Data

dbSNP Id: rs551283241
gnomAD v2: 12-62997088-G-C
gnomAD v3: 12-62603308-G-C
gnomAD v4: 12-62603308-G-C
MyVariant Identifiers: chr12:g.62997088G>C (hg19) chr12:g.62603308G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.62603308G>C , CM000674.2:g.62603308G>C GRCh38
NC_000012.11:g.62997088G>C , CM000674.1:g.62997088G>C GRCh37
NC_000012.10:g.61283355G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121682.1:n.127C>G
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