Canonical Allele Identifier: CA585077706
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1424528679
gnomAD v2: 8-128718096-A-G
gnomAD v3: 8-127705851-A-G
gnomAD v4: 8-127705851-A-G
MyVariant Identifiers: chr8:g.128718096A>G (hg19) chr8:g.127705851A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705851A>G , CM000670.2:g.127705851A>G GRCh38
NC_000008.10:g.128718096A>G , CM000670.1:g.128718096A>G GRCh37
NC_000008.9:g.128787278A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2608T>C
Search 100 bp 5'
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