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Canonical Allele Identifier:
CA12135045
Gene: LINC03000
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.164297275A>G
GRCh37
chr5:g.163724281A>G
Linked Data - Sequence & Population
gnomAD v2:
5:163724281 A / G
gnomAD v3:
5:164297275 A / G
gnomAD v4:
chr5-164297275-A-G
Joint Max Group AF
0.28823943 (EAS)
Genomes Max Group AF
0.28823943 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2964911
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.164297275A>G , CM000667.2:g.164297275A>G
GRCh38
NC_000005.9:g.163724281A>G , CM000667.1:g.163724281A>G
GRCh37
NC_000005.8:g.163656859A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001742489.1:n.501+79A>G
Search 100 bp 5'
Search 100 bp 3'