Canonical Allele Identifier: CA662381042

Gene: CUBN

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)

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