Canonical Allele Identifier: CA579528868
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1251766429
gnomAD v2: 8-2506776-T-G
gnomAD v3: 8-2649259-T-G
gnomAD v4: 8-2649259-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649259T>G , CM000670.2:g.2649259T>G GRCh38
NC_000008.10:g.2506776T>G , CM000670.1:g.2506776T>G GRCh37
NC_000008.9:g.2494183T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25471A>C