Canonical Allele Identifier: CA203630477
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs561917005
gnomAD v2: 10-17107436-T-C
gnomAD v3: 10-17065437-T-C
gnomAD v4: 10-17065437-T-C
MyVariant Identifiers: chr10:g.17107436T>C (hg19) chr10:g.17065437T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065437T>C , CM000672.2:g.17065437T>C GRCh38
NC_000010.10:g.17107436T>C , CM000672.1:g.17107436T>C GRCh37
NC_000010.9:g.17147442T>C NCBI36
NG_008967.1:g.69381A>G , LRG_540:g.69381A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.3139+71A>G MANE Select ENSP00000367064.4:n.3139+71A>G
ENST00000377833.8:c.3139+71A>G ENSP00000367064.4:n.3139+71A>G
NM_001081.3:c.3139+71A>G , LRG_540t1:c.3139+71A>G NP_001072.2:n.3139+71A>G
XM_011519708.1:c.3139+71A>G XP_011518010.1:n.3139+71A>G
XM_011519708.2:c.3139+71A>G XP_011518010.1:n.3139+71A>G
NM_001081.4:c.3139+71A>G MANE Select NP_001072.2:n.3139+71A>G
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