Canonical Allele Identifier: CA634619988
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs1390839711
gnomAD v2: 20-10850433-A-G
gnomAD v3: 20-10869785-A-G
gnomAD v4: 20-10869785-A-G
MyVariant Identifiers: chr20:g.10850433A>G (hg19) chr20:g.10869785A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869785A>G , CM000682.2:g.10869785A>G GRCh38
NC_000020.10:g.10850433A>G , CM000682.1:g.10850433A>G GRCh37
NC_000020.9:g.10798433A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2478A>G
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