Canonical Allele Identifier: CA939747502

Gene: LINC02757

Linked Data

• dbSNP Id: rs1952222867
• gnomAD v3: 11-76621172-C-T
• gnomAD v4: 11-76621172-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621172C>T , CM000673.2:g.76621172C>T	GRCh38
NC_000011.9:g.76332216C>T , CM000673.1:g.76332216C>T	GRCh37
NC_000011.8:g.76009864C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4696G>A
XR_950334.1:n.2082+5401G>A
XR_001748311.1:n.2245+4696G>A
XR_001748312.1:n.1515+4696G>A