Canonical Allele Identifier: CA1788330544
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808673042

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240392C>G , CM000670.2:g.61240392C>G GRCh38
NC_000008.10:g.62152951C>G , CM000670.1:g.62152951C>G GRCh37
NC_000008.9:g.62315505C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522621.1:c.-151-59285C>G ENSP00000428986.1:n.-151-59285C>G
XM_011517472.1:c.-151-59285C>G XP_011515774.1:n.-151-59285C>G
XM_017013141.2:c.-151-59285C>G XP_016868630.1:n.-151-59285C>G
XM_024447079.1:c.-288-51926C>G XP_024302847.1:n.-288-51926C>G