Canonical Allele Identifier: CA203618730

Gene: CUBN

Linked Data

• dbSNP Id: rs977201535
• gnomAD v2: 10-17171861-T-G
• gnomAD v3: 10-17129862-T-G
• gnomAD v4: 10-17129862-T-G
• MyVariant Identifiers: chr10:g.17171861T>G (hg19) ; chr10:g.17129862T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129862T>G , CM000672.2:g.17129862T>G	GRCh38
NC_000010.10:g.17171861T>G , CM000672.1:g.17171861T>G	GRCh37
NC_000010.9:g.17211867T>G	NCBI36
NG_008967.1:g.4956A>C , LRG_540:g.4956A>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011519708.1:c.-97A>C	XP_011518010.1:n.-97A>C
XM_011519708.2:c.-97A>C	XP_011518010.1:n.-97A>C