Allele Registry

Canonical Allele Identifier: CA15419385

Gene: LINC01411 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.174350517T>C

GRCh37 chr5:g.173777520T>C

Linked Data - Sequence & Population

gnomAD v2:

5:173777520 T / C

gnomAD v3:

5:174350517 T / C

gnomAD v4:

chr5-174350517-T-C

Joint Max Group AF 0.32541362 (EAS)

Genomes Max Group AF 0.32541362 (EAS)

Linked Data - NCBI & NCI

dbSNP:

12659144

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174350517T>C , CM000667.2:g.174350517T>C	GRCh38
NC_000005.9:g.173777520T>C , CM000667.1:g.173777520T>C	GRCh37
NC_000005.8:g.173710126T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125806.1:n.223+13941T>C

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