Canonical Allele Identifier: CA925380363
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1838730283
gnomAD v3: 10-16824934-T-C
gnomAD v4: 10-16824934-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824934T>C , CM000672.2:g.16824934T>C GRCh38
NC_000010.10:g.16866933T>C , CM000672.1:g.16866933T>C GRCh37
NC_000010.9:g.16906939T>C NCBI36
NG_008967.1:g.309884A>G , LRG_540:g.309884A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*41A>G MANE Select ENSP00000367064.4:n.*41A>G
ENST00000377833.8:c.*41A>G ENSP00000367064.4:n.*41A>G
NM_001081.3:c.*41A>G , LRG_540t1:c.*41A>G NP_001072.2:n.*41A>G
XM_011519709.1:c.*41A>G XP_011518011.1:n.*41A>G
XM_011519710.1:c.*41A>G XP_011518012.1:n.*41A>G
XM_011519711.1:c.*41A>G XP_011518013.1:n.*41A>G
XM_011519709.2:c.*41A>G XP_011518011.1:n.*41A>G
XM_011519710.2:c.*41A>G XP_011518012.1:n.*41A>G
XM_011519711.3:c.*41A>G XP_011518013.1:n.*41A>G
NM_001081.4:c.*41A>G MANE Select NP_001072.2:n.*41A>G
Search 100 bp 5'
Search 100 bp 3'