Canonical Allele Identifier: CA1788330466
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1354286677

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240287T>C , CM000670.2:g.61240287T>C GRCh38
NC_000008.10:g.62152846T>C , CM000670.1:g.62152846T>C GRCh37
NC_000008.9:g.62315400T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522621.1:c.-151-59390T>C ENSP00000428986.1:n.-151-59390T>C
XM_011517472.1:c.-151-59390T>C XP_011515774.1:n.-151-59390T>C
XM_017013141.2:c.-151-59390T>C XP_016868630.1:n.-151-59390T>C
XM_024447079.1:c.-288-52031T>C XP_024302847.1:n.-288-52031T>C