Canonical Allele Identifier: CA662376633
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1346746084
gnomAD v4: 10-17065409-C-T
MyVariant Identifiers: chr10:g.17107408C>T (hg19) chr10:g.17065409C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065409C>T , CM000672.2:g.17065409C>T GRCh38
NC_000010.10:g.17107408C>T , CM000672.1:g.17107408C>T GRCh37
NC_000010.9:g.17147414C>T NCBI36
NG_008967.1:g.69409G>A , LRG_540:g.69409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.3139+99G>A MANE Select ENSP00000367064.4:n.3139+99G>A
ENST00000377833.8:c.3139+99G>A ENSP00000367064.4:n.3139+99G>A
NM_001081.3:c.3139+99G>A , LRG_540t1:c.3139+99G>A NP_001072.2:n.3139+99G>A
XM_011519708.1:c.3139+99G>A XP_011518010.1:n.3139+99G>A
XM_011519708.2:c.3139+99G>A XP_011518010.1:n.3139+99G>A
NM_001081.4:c.3139+99G>A MANE Select NP_001072.2:n.3139+99G>A
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