Canonical Allele Identifier: CA136296481
Gene: CASC15 HGNC NCBI

Linked Data

dbSNP Id: rs773546275
gnomAD v2: 6-22131903-T-G
gnomAD v3: 6-22131674-T-G
gnomAD v4: 6-22131674-T-G
MyVariant Identifiers: chr6:g.22131903T>G (hg19) chr6:g.22131674T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22131674T>G , CM000668.2:g.22131674T>G GRCh38
NC_000006.11:g.22131903T>G , CM000668.1:g.22131903T>G GRCh37
NC_000006.10:g.22239882T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+20754T>G
NR_015410.2:n.1422+20754T>G
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