Canonical Allele Identifier: CA836611524

Gene: LINC01162

Linked Data

• dbSNP Id: rs1212526774
• MyVariant Identifiers: chr7:g.20994405_20994406del (hg19) ; chr7:g.20954786_20954787del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954786_20954787del , CM000669.2:g.20954786_20954787del	GRCh38
NC_000007.13:g.20994405_20994406del , CM000669.1:g.20994405_20994406del	GRCh37
NC_000007.12:g.20960930_20960931del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.152-66082_152-66081del