Canonical Allele Identifier: CA85231833
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs901378668
gnomAD v2: 3-147935545-T-G
gnomAD v3: 3-148217758-T-G
gnomAD v4: 3-148217758-T-G
MyVariant Identifiers: chr3:g.147935545T>G (hg19) chr3:g.148217758T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217758T>G , CM000665.2:g.148217758T>G GRCh38
NC_000003.11:g.147935545T>G , CM000665.1:g.147935545T>G GRCh37
NC_000003.10:g.149418235T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2752A>C
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