Canonical Allele Identifier: CA662381042
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1451965085
gnomAD v3: 10-17129854-T-C
gnomAD v4: 10-17129854-T-C
MyVariant Identifiers: chr10:g.17171853T>C (hg19) chr10:g.17129854T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129854T>C , CM000672.2:g.17129854T>C GRCh38
NC_000010.10:g.17171853T>C , CM000672.1:g.17171853T>C GRCh37
NC_000010.9:g.17211859T>C NCBI36
NG_008967.1:g.4964A>G , LRG_540:g.4964A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011519708.1:c.-89A>G XP_011518010.1:n.-89A>G
XM_011519708.2:c.-89A>G XP_011518010.1:n.-89A>G
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