Canonical Allele Identifier: CA853946856
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1298956213

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240292A>G , CM000670.2:g.61240292A>G GRCh38
NC_000008.10:g.62152851A>G , CM000670.1:g.62152851A>G GRCh37
NC_000008.9:g.62315405A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522621.1:c.-151-59385A>G ENSP00000428986.1:n.-151-59385A>G
XM_011517472.1:c.-151-59385A>G XP_011515774.1:n.-151-59385A>G
XM_017013141.2:c.-151-59385A>G XP_016868630.1:n.-151-59385A>G
XM_024447079.1:c.-288-52026A>G XP_024302847.1:n.-288-52026A>G