Canonical Allele Identifier: CA646775023
Gene: LINC01794 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.40761826G>A , CM000664.2:g.40761826G>A GRCh38
NC_000002.11:g.40988966G>A , CM000664.1:g.40988966G>A GRCh37
NC_000002.10:g.40842470G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939988.1:n.246+6607G>A
XR_939989.1:n.247-5390G>A
XR_939990.1:n.247-2431G>A
XR_939994.1:n.217-64899C>T
XR_939995.1:n.217-64899C>T
XR_001739421.2:n.217-64899C>T
XR_001739422.1:n.1666-64899C>T
XR_001739423.1:n.217-23674C>T
XR_002959380.1:n.692-2431G>A
XR_939989.3:n.226-5390G>A
XR_939994.2:n.217-64899C>T
XR_939995.2:n.217-64899C>T