Canonical Allele Identifier: CA1869205434
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261880_103261882delinsAAC , CM000671.2:g.103261880_103261882delinsAAC GRCh38
NC_000009.11:g.106024162_106024164delinsAAC , CM000671.1:g.106024162_106024164delinsAAC GRCh37
NC_000009.10:g.105063983_105063985delinsAAC NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2642_771+2644delinsGTT