Canonical Allele Identifier: CA85231870
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs200433317
gnomAD v2: 3-147935678-TC-T
gnomAD v3: 3-148217891-TC-T
gnomAD v4: 3-148217891-TC-T
MyVariant Identifiers: chr3:g.147935679del (hg19) chr3:g.148217892del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217892del , CM000665.2:g.148217892del GRCh38
NC_000003.11:g.147935679del , CM000665.1:g.147935679del GRCh37
NC_000003.10:g.149418369del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2618del
Search 100 bp 5'
Search 100 bp 3'