Canonical Allele Identifier: CA1743017243
Gene: UBE2H HGNC NCBI

Linked Data

dbSNP Id: rs1805380810

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129839104G>T , CM000669.2:g.129839104G>T GRCh38
NC_000007.13:g.129478944G>T , CM000669.1:g.129478944G>T GRCh37
NC_000007.12:g.129266180G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355621.8:c.427+103C>A MANE Select ENSP00000347836.3:n.427+103C>A
ENST00000649897.1:c.217+103C>A ENSP00000497987.1:n.217+103C>A
ENST00000355621.7:c.427+103C>A ENSP00000347836.3:n.427+103C>A
ENST00000473814.6:c.334+103C>A ENSP00000419097.2:n.334+103C>A
ENST00000483368.1:n.535+103C>A
ENST00000496698.5:c.328+103C>A ENSP00000417681.1:n.328+103C>A
NM_001202498.1:c.217+103C>A NP_001189427.1:n.217+103C>A
NM_003344.3:c.427+103C>A NP_003335.1:n.427+103C>A
NM_182697.2:c.334+103C>A NP_874356.1:n.334+103C>A
XM_011516547.1:c.616+103C>A XP_011514849.1:n.616+103C>A
NM_001202498.2:c.217+103C>A NP_001189427.1:n.217+103C>A
NM_003344.4:c.427+103C>A MANE Select NP_003335.1:n.427+103C>A
NM_182697.3:c.334+103C>A NP_874356.1:n.334+103C>A