Canonical Allele Identifier: CA59146127
Gene: LINC01876 HGNC NCBI

Linked Data

dbSNP Id: rs17188434

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156240264T>C , CM000664.2:g.156240264T>C GRCh38
NC_000002.11:g.157096776T>C , CM000664.1:g.157096776T>C GRCh37
NC_000002.10:g.156805022T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110249.2:n.154+14514A>G
NR_110250.2:n.154+14514A>G
XR_923502.1:n.1303-12260A>G