Canonical Allele Identifier: CA1993253464
Gene: MAML2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.96259000T= , CM000673.2:g.96259000T= GRCh38
NC_000011.9:g.95992164T= , CM000673.1:g.95992164T= GRCh37
NC_000011.8:g.95631812T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524717.6:c.513+82383A= MANE Select ENSP00000434552.1:n.513+82383A=
ENST00000524717.5:c.513+82383A= ENSP00000434552.1:n.513+82383A=
NM_032427.3:c.513+82383A= NP_115803.1:n.513+82383A=
XM_011543024.1:c.-172+83908A= XP_011541326.1:n.-172+83908A=
XM_011543025.1:c.513+82383A= XP_011541327.1:n.513+82383A=
XM_011543024.3:c.-172+83908A= XP_011541326.1:n.-172+83908A=
XM_011543025.2:c.513+82383A= XP_011541327.1:n.513+82383A=
NM_032427.4:c.513+82383A= MANE Select NP_115803.1:n.513+82383A=
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