Canonical Allele Identifier: CA1230641171
Gene: LINC02774 HGNC NCBI

Linked Data

dbSNP Id: rs10927101

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244010570C>G , CM000663.2:g.244010570C>G GRCh38
NC_000001.10:g.244173872C>G , CM000663.1:g.244173872C>G GRCh37
NC_000001.9:g.242240495C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033883.1:n.527-127C>G