Canonical Allele Identifier: CA1623081778
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1581657151
gnomAD v3: 6-40354221-G-A
gnomAD v4: 6-40354221-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354221G>A , CM000668.2:g.40354221G>A GRCh38
NC_000006.11:g.40321960G>A , CM000668.1:g.40321960G>A GRCh37
NC_000006.10:g.40429938G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1786C>T
Search 100 bp 5'
Search 100 bp 3'