Canonical Allele Identifier: CA1893472802
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1588663425

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129848T>G , CM000672.2:g.17129848T>G GRCh38
NC_000010.10:g.17171847T>G , CM000672.1:g.17171847T>G GRCh37
NC_000010.9:g.17211853T>G NCBI36
NG_008967.1:g.4970A>C , LRG_540:g.4970A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011519708.1:c.-83A>C XP_011518010.1:n.-83A>C
XM_011519708.2:c.-83A>C XP_011518010.1:n.-83A>C