Canonical Allele Identifier: CA2162093
Gene: LINC00471 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.231513520T>C
GRCh37 chr2:g.232378231T>C
gnomAD v2:
2:232378231 T / C
gnomAD v3:
2:231513520 T / C
gnomAD v4:
chr2-231513520-T-C
Joint Max Group AF 0.71150601 (EAS)
Genomes Max Group AF 0.7067548 (EAS)
Exomes Max Group AF 0.707969 (EAS)
dbSNP:
6750795
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.231513520T>C , CM000664.2:g.231513520T>C GRCh38
NC_000002.11:g.232378231T>C , CM000664.1:g.232378231T>C GRCh37
NC_000002.10:g.232086475T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024079.1:n.364+7A>G
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