Canonical Allele Identifier: CA582286358
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1354286677
gnomAD v2: 8-62152846-T-A

Genomic Alleles

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

Transcript Alleles

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