Canonical Allele Identifier: CA836611527

Gene: LINC01162

Linked Data

• dbSNP Id: rs1309775281
• gnomAD v3: 7-20954796-A-T
• gnomAD v4: 7-20954796-A-T
• MyVariant Identifiers: chr7:g.20994415A>T (hg19) ; chr7:g.20954796A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954796A>T , CM000669.2:g.20954796A>T	GRCh38
NC_000007.13:g.20994415A>T , CM000669.1:g.20994415A>T	GRCh37
NC_000007.12:g.20960940A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_126381.1:n.152-66072A>T