Canonical Allele Identifier: CA229613684

Gene: LINC02744

Linked Data

• dbSNP Id: rs72645475
• gnomAD v2: 11-119863615-G-A
• gnomAD v3: 11-119992906-G-A
• gnomAD v4: 11-119992906-G-A
• MyVariant Identifiers: chr11:g.119863615G>A (hg19) ; chr11:g.119992906G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119992906G>A , CM000673.2:g.119992906G>A	GRCh38
NC_000011.9:g.119863615G>A , CM000673.1:g.119863615G>A	GRCh37
NC_000011.8:g.119368825G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948086.1:n.480C>T
XR_948087.1:n.199+1688C>T
XR_948090.1:n.176+1688C>T
XR_948091.1:n.177+1688C>T
XR_948093.1:n.177+1688C>T
XR_948094.1:n.175+1688C>T
XR_948096.1:n.174+1688C>T
XR_002957267.1:n.2019C>T
XR_948086.2:n.572C>T
XR_948087.2:n.346+1688C>T
XR_948088.3:n.2022C>T
XR_948089.3:n.2020C>T
XR_948090.2:n.338+1688C>T
XR_948091.2:n.340+1688C>T
XR_948092.3:n.2021C>T