Canonical Allele Identifier: CA853946901
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs1488905532
MyVariant Identifiers: chr8:g.62152927G>A (hg19) chr8:g.61240368G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240368G>A , CM000670.2:g.61240368G>A GRCh38
NC_000008.10:g.62152927G>A , CM000670.1:g.62152927G>A GRCh37
NC_000008.9:g.62315481G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522621.1:c.-151-59309G>A ENSP00000428986.1:n.-151-59309G>A
XM_011517472.1:c.-151-59309G>A XP_011515774.1:n.-151-59309G>A
XM_017013141.2:c.-151-59309G>A XP_016868630.1:n.-151-59309G>A
XM_024447079.1:c.-288-51950G>A XP_024302847.1:n.-288-51950G>A
Search 100 bp 5'
Search 100 bp 3'