Canonical Allele Identifier: CA1247082278
Gene: LINC01794 HGNC NCBI

Linked Data

dbSNP Id: rs1667528447

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.40761829G>A , CM000664.2:g.40761829G>A GRCh38
NC_000002.11:g.40988969G>A , CM000664.1:g.40988969G>A GRCh37
NC_000002.10:g.40842473G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939988.1:n.246+6610G>A
XR_939989.1:n.247-5387G>A
XR_939990.1:n.247-2428G>A
XR_939994.1:n.217-64902C>T
XR_939995.1:n.217-64902C>T
XR_001739421.2:n.217-64902C>T
XR_001739422.1:n.1666-64902C>T
XR_001739423.1:n.217-23677C>T
XR_002959380.1:n.692-2428G>A
XR_939989.3:n.226-5387G>A
XR_939994.2:n.217-64902C>T
XR_939995.2:n.217-64902C>T