Canonical Allele Identifier: CA2595736959
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs2113770963
gnomAD v3: 6-40354009-G-T
gnomAD v4: 6-40354009-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354009G>T , CM000668.2:g.40354009G>T GRCh38
NC_000006.11:g.40321748G>T , CM000668.1:g.40321748G>T GRCh37
NC_000006.10:g.40429726G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1998C>A