Canonical Allele Identifier: CA582286366
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1216227913
gnomAD v2: 8-62152920-T-C
gnomAD v3: 8-61240361-T-C
gnomAD v4: 8-61240361-T-C
MyVariant Identifiers: chr8:g.62152920T>C (hg19) chr8:g.61240361T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240361T>C , CM000670.2:g.61240361T>C GRCh38
NC_000008.10:g.62152920T>C , CM000670.1:g.62152920T>C GRCh37
NC_000008.9:g.62315474T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000522621.1:c.-151-59316T>C ENSP00000428986.1:n.-151-59316T>C
XM_011517472.1:c.-151-59316T>C XP_011515774.1:n.-151-59316T>C
XM_017013141.2:c.-151-59316T>C XP_016868630.1:n.-151-59316T>C
XM_024447079.1:c.-288-51957T>C XP_024302847.1:n.-288-51957T>C
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