Canonical Allele Identifier: CA557298363
Gene: LINC02515 HGNC NCBI

Linked Data

dbSNP Id: rs1195266496
gnomAD v2: 4-188345340-G-A
gnomAD v3: 4-187424186-G-A
gnomAD v4: 4-187424186-G-A
MyVariant Identifiers: chr4:g.188345340G>A (hg19) chr4:g.187424186G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.187424186G>A , CM000666.2:g.187424186G>A GRCh38
NC_000004.11:g.188345340G>A , CM000666.1:g.188345340G>A GRCh37
NC_000004.10:g.188582334G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038931.1:n.322+81106C>T
XR_939603.1:n.268+1189G>A
XR_001741954.1:n.258+10475G>A
XR_001741955.1:n.1517+1189G>A
XR_001741956.1:n.258+10475G>A
XR_939603.2:n.269+1189G>A
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