Canonical Allele Identifier: CA1088160951
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762012638
gnomAD v3: 6-40353978-G-T
gnomAD v4: 6-40353978-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353978G>T , CM000668.2:g.40353978G>T GRCh38
NC_000006.11:g.40321717G>T , CM000668.1:g.40321717G>T GRCh37
NC_000006.10:g.40429695G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2029C>A