Canonical Allele Identifier: CA1893472799
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1837279013

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129843G>A , CM000672.2:g.17129843G>A GRCh38
NC_000010.10:g.17171842G>A , CM000672.1:g.17171842G>A GRCh37
NC_000010.9:g.17211848G>A NCBI36
NG_008967.1:g.4975C>T , LRG_540:g.4975C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011519708.1:c.-78C>T XP_011518010.1:n.-78C>T
XM_011519708.2:c.-78C>T XP_011518010.1:n.-78C>T