Canonical Allele Identifier: CA178268070
Gene: CLVS1 HGNC NCBI

Linked Data

dbSNP Id: rs529932500
gnomAD v2: 8-62152804-G-A
gnomAD v3: 8-61240245-G-A
gnomAD v4: 8-61240245-G-A
MyVariant Identifiers: chr8:g.62152804G>A (hg19) chr8:g.61240245G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.61240245G>A , CM000670.2:g.61240245G>A GRCh38
NC_000008.10:g.62152804G>A , CM000670.1:g.62152804G>A GRCh37
NC_000008.9:g.62315358G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522621.1:c.-151-59432G>A ENSP00000428986.1:n.-151-59432G>A
XM_011517472.1:c.-151-59432G>A XP_011515774.1:n.-151-59432G>A
XM_017013141.2:c.-151-59432G>A XP_016868630.1:n.-151-59432G>A
XM_024447079.1:c.-288-52073G>A XP_024302847.1:n.-288-52073G>A
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