Canonical Allele Identifier: CA48805975

Gene: LINC01122

Linked Data

• dbSNP Id: rs6719884
• gnomAD v2: 2-59036916-A-C
• gnomAD v3: 2-58809781-A-C
• gnomAD v4: 2-58809781-A-C
• MyVariant Identifiers: chr2:g.59036916A>C (hg19) ; chr2:g.58809781A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.58809781A>C , CM000664.2:g.58809781A>C	GRCh38
NC_000002.11:g.59036916A>C , CM000664.1:g.59036916A>C	GRCh37
NC_000002.10:g.58890420A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_033873.1:n.248-40649A>C