Canonical Allele Identifier: CA10628653
Gene: LMBR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 359445
ClinVar RCV Id: RCV000402824 RCV001709631
dbSNP Id: rs528727956
gnomAD v2: 7-156685901-T-TCGGGGGCGGGG
gnomAD v3: 7-156893207-T-TCGGGGGCGGGG
gnomAD v4: 7-156893207-T-TCGGGGGCGGGG
MyVariant Identifiers: chr7:g.156685912_156685913insCGGGGGCGGGG (hg19) chr7:g.156685901_156685902insCGGGGGCGGGG (hg19) chr7:g.156893218_156893219insCGGGGGCGGGG (hg38) chr7:g.156893207_156893208insCGGGGGCGGGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.156893220_156893230dup , CM000669.2:g.156893220_156893230dup GRCh38
NC_000007.13:g.156685914_156685924dup , CM000669.1:g.156685914_156685924dup GRCh37
NC_000007.12:g.156378675_156378685dup NCBI36
NG_009240.1:g.4991_5001dup
NG_009240.2:g.4991_5001dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000353442.9:c.-225_-215dup ENSP00000326604.7:n.-225_-215dup
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