Canonical Allele Identifier: CA530384467

Gene: LINC02774

Linked Data

• dbSNP Id: rs10927101
• gnomAD v2: 1-244173872-C-T
• gnomAD v3: 1-244010570-C-T
• gnomAD v4: 1-244010570-C-T
• MyVariant Identifiers: chr1:g.244173872C>T (hg19) ; chr1:g.244010570C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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