Canonical Allele Identifier: CA1114472171
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808665136
gnomAD v3: 8-61240286-G-C
gnomAD v4: 8-61240286-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240286G>C , CM000670.2:g.61240286G>C GRCh38
NC_000008.10:g.62152845G>C , CM000670.1:g.62152845G>C GRCh37
NC_000008.9:g.62315399G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000522621.1:c.-151-59391G>C ENSP00000428986.1:n.-151-59391G>C
XM_011517472.1:c.-151-59391G>C XP_011515774.1:n.-151-59391G>C
XM_017013141.2:c.-151-59391G>C XP_016868630.1:n.-151-59391G>C
XM_024447079.1:c.-288-52032G>C XP_024302847.1:n.-288-52032G>C
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