Canonical Allele Identifier: CA697877541
Gene: LINC02334 HGNC NCBI

Linked Data

dbSNP Id: rs1222171820
MyVariant Identifiers: chr13:g.38531600G>A (hg19) chr13:g.37957463G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.37957463G>A , CM000675.2:g.37957463G>A GRCh38
NC_000013.10:g.38531600G>A , CM000675.1:g.38531600G>A GRCh37
NC_000013.9:g.37429600G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941877.1:n.466+22426G>A
XR_941878.1:n.466+22426G>A
XR_941879.1:n.466+22426G>A
XR_941880.1:n.466+22426G>A
XR_941881.1:n.466+22426G>A
XR_941882.1:n.325+22567G>A
XR_941877.2:n.536+22426G>A
XR_941880.3:n.539+22426G>A
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