Canonical Allele Identifier: CA12739454
Gene: CASC21 HGNC NCBI
CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs16902094
gnomAD v2: 8-128320346-A-G
gnomAD v3: 8-127308101-A-G
gnomAD v4: 8-127308101-A-G
MyVariant Identifiers: chr8:g.128320346A>G (hg19) chr8:g.127308101A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127308101A>G , CM000670.2:g.127308101A>G GRCh38
NC_000008.10:g.128320346A>G , CM000670.1:g.128320346A>G GRCh37
NC_000008.9:g.128389528A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117099.1:n.149-13972A>G (CASC21)
NR_117100.1:n.1177-18041T>C (CASC8)
Search 100 bp 5'
Search 100 bp 3'