Canonical Allele Identifier: CA1054734349
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712874312
gnomAD v3: 3-148217861-C-A
gnomAD v4: 3-148217861-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217861C>A , CM000665.2:g.148217861C>A GRCh38
NC_000003.11:g.147935648C>A , CM000665.1:g.147935648C>A GRCh37
NC_000003.10:g.149418338C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924565.1:n.86+2649G>T
Search 100 bp 5'
Search 100 bp 3'