ClinGen Allele Registry
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Canonical Allele Identifier:
CA1109725465
Gene: LINC03021
HGNC
NCBI
Linked Data
dbSNP Id:
rs1003097920
gnomAD v3:
8-2649209-G-C
gnomAD v4:
8-2649209-G-C
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.2649209G>C , CM000670.2:g.2649209G>C
GRCh38
NC_000008.10:g.2506726G>C , CM000670.1:g.2506726G>C
GRCh37
NC_000008.9:g.2494133G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125425.1:n.238+25521C>G
Search 100 bp 5'
Search 100 bp 3'