Canonical Allele Identifier: CA29935947
Gene: LINC00624 HGNC NCBI

Linked Data

dbSNP Id: rs4950322

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147383114G>A , CM000663.2:g.147383114G>A GRCh38
NC_000001.10:g.146854836G>A , CM000663.1:g.146854836G>A GRCh37
NC_000001.9:g.145321460G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038423.2:n.2450C>T