Canonical Allele Identifier: CA10758849

Gene: LINC02774

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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