Canonical Allele Identifier: CA480537627

Gene: LINC01465

Linked Data

• dbSNP Id: rs1431769031
• gnomAD v4: 12-62603306-C-T
• MyVariant Identifiers: chr12:g.62997086C>T (hg19) ; chr12:g.62603306C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.62603306C>T , CM000674.2:g.62603306C>T	GRCh38
NC_000012.11:g.62997086C>T , CM000674.1:g.62997086C>T	GRCh37
NC_000012.10:g.61283353C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121682.1:n.129G>A