Canonical Allele Identifier: CA1993195784
Gene: MAML2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.96133500C= , CM000673.2:g.96133500C= GRCh38
NC_000011.9:g.95866664C= , CM000673.1:g.95866664C= GRCh37
NC_000011.8:g.95506312C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524717.6:c.514-39983G= MANE Select ENSP00000434552.1:n.514-39983G=
ENST00000524717.5:c.514-39983G= ENSP00000434552.1:n.514-39983G=
NM_032427.3:c.514-39983G= NP_115803.1:n.514-39983G=
XM_011543023.1:c.73-39983G= XP_011541325.1:n.73-39983G=
XM_011543024.1:c.-171-39983G= XP_011541326.1:n.-171-39983G=
XM_011543025.1:c.514-39983G= XP_011541327.1:n.514-39983G=
XM_011543023.3:c.73-39983G= XP_011541325.1:n.73-39983G=
XM_011543024.3:c.-171-39983G= XP_011541326.1:n.-171-39983G=
XM_011543025.2:c.514-39983G= XP_011541327.1:n.514-39983G=
NM_032427.4:c.514-39983G= MANE Select NP_115803.1:n.514-39983G=
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