Canonical Allele Identifier: CA1099137360

Gene: LINC01162

Linked Data

• dbSNP Id: rs1418715934
• gnomAD v3: 7-20845411-C-T
• gnomAD v4: 7-20845411-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845411C>T , CM000669.2:g.20845411C>T	GRCh38
NC_000007.13:g.20885030C>T , CM000669.1:g.20885030C>T	GRCh37
NC_000007.12:g.20851555C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9907C>T