Canonical Allele Identifier: CA535050369
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1330052652

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219219_100219221del , CM000664.2:g.100219219_100219221del GRCh38
NC_000002.11:g.100835681_100835683del , CM000664.1:g.100835681_100835683del GRCh37
NC_000002.10:g.100202113_100202115del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10399_567+10401del