Canonical Allele Identifier: CA2651924472
Gene: LINC00687 HGNC NCBI

Linked Data

gnomAD v4: 20-11810136-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810136T>C , CM000682.2:g.11810136T>C GRCh38
NC_000020.10:g.11790784T>C , CM000682.1:g.11790784T>C GRCh37
NC_000020.9:g.11738784T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110635.1:n.375A>G
Search 100 bp 5'
Search 100 bp 3'