Canonical Allele Identifier: CA779420764
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1462250248
gnomAD v3: 18-42470272-GT-G
gnomAD v4: 18-42470272-GT-G
MyVariant Identifiers: chr18:g.40050238del (hg19) chr18:g.42470273del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470274del , CM000680.2:g.42470274del GRCh38
NC_000018.9:g.40050239del , CM000680.1:g.40050239del GRCh37
NC_000018.8:g.38304237del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15285del
NR_046454.1:n.652+15285del
NR_046455.1:n.489+15285del
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