Canonical Allele Identifier: CA155651887
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs540100770
gnomAD v3: 7-20954913-C-T
gnomAD v4: 7-20954913-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954913C>T , CM000669.2:g.20954913C>T GRCh38
NC_000007.13:g.20994532C>T , CM000669.1:g.20994532C>T GRCh37
NC_000007.12:g.20961057C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65955C>T