Canonical Allele Identifier: CA10737808
Gene: LINC01780 HGNC NCBI

Linked Data

dbSNP Id: rs17023457

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119333107T>C , CM000663.2:g.119333107T>C GRCh38
NC_000001.10:g.119875730T>C , CM000663.1:g.119875730T>C GRCh37
NC_000001.9:g.119677253T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947752.1:n.919+4318T>C
XR_947753.1:n.919+4318T>C
XR_947754.1:n.919+4318T>C
NR_146623.1:n.82+4318T>C