Canonical Allele Identifier: CA915290490
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1561825183
gnomAD v2: 6-40321625-G-A
gnomAD v3: 6-40353886-G-A
gnomAD v4: 6-40353886-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353886G>A , CM000668.2:g.40353886G>A GRCh38
NC_000006.11:g.40321625G>A , CM000668.1:g.40321625G>A GRCh37
NC_000006.10:g.40429603G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2121C>T
Search 100 bp 5'
Search 100 bp 3'