Canonical Allele Identifier: CA1247082275
Gene: LINC01794 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.40761828T= , CM000664.2:g.40761828T= GRCh38
NC_000002.11:g.40988968T= , CM000664.1:g.40988968T= GRCh37
NC_000002.10:g.40842472T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939988.1:n.246+6609T=
XR_939989.1:n.247-5388T=
XR_939990.1:n.247-2429T=
XR_939994.1:n.217-64901A=
XR_939995.1:n.217-64901A=
XR_001739421.2:n.217-64901A=
XR_001739422.1:n.1666-64901A=
XR_001739423.1:n.217-23676A=
XR_002959380.1:n.692-2429T=
XR_939989.3:n.226-5388T=
XR_939994.2:n.217-64901A=
XR_939995.2:n.217-64901A=