Canonical Allele Identifier: CA662381045
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1292012862
gnomAD v3: 10-17129860-C-T
gnomAD v4: 10-17129860-C-T
MyVariant Identifiers: chr10:g.17171859C>T (hg19) chr10:g.17129860C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129860C>T , CM000672.2:g.17129860C>T GRCh38
NC_000010.10:g.17171859C>T , CM000672.1:g.17171859C>T GRCh37
NC_000010.9:g.17211865C>T NCBI36
NG_008967.1:g.4958G>A , LRG_540:g.4958G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011519708.1:c.-95G>A XP_011518010.1:n.-95G>A
XM_011519708.2:c.-95G>A XP_011518010.1:n.-95G>A
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