Canonical Allele Identifier: CA532160202

Gene: LINC01794

Linked Data

• dbSNP Id: rs1281686666
• gnomAD v2: 2-40988991-G-T
• gnomAD v3: 2-40761851-G-T
• gnomAD v4: 2-40761851-G-T
• MyVariant Identifiers: chr2:g.40988991G>T (hg19) ; chr2:g.40761851G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.40761851G>T , CM000664.2:g.40761851G>T	GRCh38
NC_000002.11:g.40988991G>T , CM000664.1:g.40988991G>T	GRCh37
NC_000002.10:g.40842495G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939988.1:n.246+6632G>T
XR_939989.1:n.247-5365G>T
XR_939990.1:n.247-2406G>T
XR_939994.1:n.217-64924C>A
XR_939995.1:n.217-64924C>A
XR_001739421.2:n.217-64924C>A
XR_001739422.1:n.1666-64924C>A
XR_001739423.1:n.217-23699C>A
XR_002959380.1:n.692-2406G>T
XR_939989.3:n.226-5365G>T
XR_939994.2:n.217-64924C>A
XR_939995.2:n.217-64924C>A