Canonical Allele Identifier: CA1863645091
Gene: LINC00484 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91166134C>G , CM000671.2:g.91166134C>G GRCh38
NC_000009.11:g.93928416C>G , CM000671.1:g.93928416C>G GRCh37
NC_000009.10:g.92968237C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930113.1:n.264-4539C>G
XR_930114.1:n.268-4539C>G
XR_930115.1:n.259-4539C>G
XR_930116.1:n.618-4539C>G
XR_930117.1:n.597-4539C>G
NR_135306.1:n.161-16335C>G