Canonical Allele Identifier: CA1114472175
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808672762
gnomAD v3: 8-61240379-C-A
gnomAD v4: 8-61240379-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240379C>A , CM000670.2:g.61240379C>A GRCh38
NC_000008.10:g.62152938C>A , CM000670.1:g.62152938C>A GRCh37
NC_000008.9:g.62315492C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000522621.1:c.-151-59298C>A ENSP00000428986.1:n.-151-59298C>A
XM_011517472.1:c.-151-59298C>A XP_011515774.1:n.-151-59298C>A
XM_017013141.2:c.-151-59298C>A XP_016868630.1:n.-151-59298C>A
XM_024447079.1:c.-288-51939C>A XP_024302847.1:n.-288-51939C>A
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