Canonical Allele Identifier: CA203618735
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs924353061
gnomAD v3: 10-17129867-T-A
gnomAD v4: 10-17129867-T-A
MyVariant Identifiers: chr10:g.17171866T>A (hg19) chr10:g.17129867T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129867T>A , CM000672.2:g.17129867T>A GRCh38
NC_000010.10:g.17171866T>A , CM000672.1:g.17171866T>A GRCh37
NC_000010.9:g.17211872T>A NCBI36
NG_008967.1:g.4951A>T , LRG_540:g.4951A>T

Transcript Alleles

HGVS Amino-acid Change
XM_011519708.1:c.-102A>T XP_011518010.1:n.-102A>T
XM_011519708.2:c.-102A>T XP_011518010.1:n.-102A>T
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