Canonical Allele Identifier: CA178268169
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1043060367
gnomAD v3: 8-61240352-C-T
gnomAD v4: 8-61240352-C-T
MyVariant Identifiers: chr8:g.62152911C>T (hg19) chr8:g.61240352C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240352C>T , CM000670.2:g.61240352C>T GRCh38
NC_000008.10:g.62152911C>T , CM000670.1:g.62152911C>T GRCh37
NC_000008.9:g.62315465C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522621.1:c.-151-59325C>T ENSP00000428986.1:n.-151-59325C>T
XM_011517472.1:c.-151-59325C>T XP_011515774.1:n.-151-59325C>T
XM_017013141.2:c.-151-59325C>T XP_016868630.1:n.-151-59325C>T
XM_024447079.1:c.-288-51966C>T XP_024302847.1:n.-288-51966C>T
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