Canonical Allele Identifier: CA203618733

Gene: CUBN

Linked Data

• dbSNP Id: rs145233594
• gnomAD v3: 10-17129866-A-C
• gnomAD v4: 10-17129866-A-C
• MyVariant Identifiers: chr10:g.17171865A>C (hg19) ; chr10:g.17129866A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129866A>C , CM000672.2:g.17129866A>C	GRCh38
NC_000010.10:g.17171865A>C , CM000672.1:g.17171865A>C	GRCh37
NC_000010.9:g.17211871A>C	NCBI36
NG_008967.1:g.4952T>G , LRG_540:g.4952T>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011519708.1:c.-101T>G	XP_011518010.1:n.-101T>G
XM_011519708.2:c.-101T>G	XP_011518010.1:n.-101T>G