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Canonical Allele Identifier:
CA170532281
Gene: LINC03021
HGNC
NCBI
Linked Data
dbSNP Id:
rs1047590251
MyVariant Identifiers:
chr8:g.2506801T>G (hg19)
chr8:g.2649284T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.2649284T>G , CM000670.2:g.2649284T>G
GRCh38
NC_000008.10:g.2506801T>G , CM000670.1:g.2506801T>G
GRCh37
NC_000008.9:g.2494208T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_125425.1:n.238+25446A>C
Search 100 bp 5'
Search 100 bp 3'