Canonical Allele Identifier: CA1869205453
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261923T= , CM000671.2:g.103261923T= GRCh38
NC_000009.11:g.106024205T= , CM000671.1:g.106024205T= GRCh37
NC_000009.10:g.105064026T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2601A=