Canonical Allele Identifier: CA2595736960
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs2113770976
gnomAD v3: 6-40354021-G-A
gnomAD v4: 6-40354021-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354021G>A , CM000668.2:g.40354021G>A GRCh38
NC_000006.11:g.40321760G>A , CM000668.1:g.40321760G>A GRCh37
NC_000006.10:g.40429738G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1986C>T