Canonical Allele Identifier: CA137815811

Gene: LINC00951

Linked Data

• dbSNP Id: rs900864063
• gnomAD v2: 6-40321970-G-A
• gnomAD v3: 6-40354231-G-A
• gnomAD v4: 6-40354231-G-A
• MyVariant Identifiers: chr6:g.40321970G>A (hg19) ; chr6:g.40354231G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354231G>A , CM000668.2:g.40354231G>A	GRCh38
NC_000006.11:g.40321970G>A , CM000668.1:g.40321970G>A	GRCh37
NC_000006.10:g.40429948G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1776C>T