Canonical Allele Identifier: CA136833343
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1030792155
gnomAD v2: 6-31274458-C-G
gnomAD v3: 6-31306681-C-G
gnomAD v4: 6-31306681-C-G
MyVariant Identifiers: chr6:g.31274458C>G (hg19) chr6:g.31306681C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306681C>G , CM000668.2:g.31306681C>G GRCh38
NC_000006.11:g.31274458C>G , CM000668.1:g.31274458C>G GRCh37
NC_000006.10:g.31382437C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+97G>C
XR_926691.2:n.965+97G>C
Search 100 bp 5'
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