Canonical Allele Identifier: CA682243619
Gene: MAML2 HGNC NCBI

Linked Data

dbSNP Id: rs11021499
MyVariant Identifiers: chr11:g.95992129G>T (hg19) chr11:g.96258965G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.96258965G>T , CM000673.2:g.96258965G>T GRCh38
NC_000011.9:g.95992129G>T , CM000673.1:g.95992129G>T GRCh37
NC_000011.8:g.95631777G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524717.6:c.513+82418C>A MANE Select ENSP00000434552.1:n.513+82418C>A
ENST00000524717.5:c.513+82418C>A ENSP00000434552.1:n.513+82418C>A
NM_032427.3:c.513+82418C>A NP_115803.1:n.513+82418C>A
XM_011543024.1:c.-172+83943C>A XP_011541326.1:n.-172+83943C>A
XM_011543025.1:c.513+82418C>A XP_011541327.1:n.513+82418C>A
XM_011543024.3:c.-172+83943C>A XP_011541326.1:n.-172+83943C>A
XM_011543025.2:c.513+82418C>A XP_011541327.1:n.513+82418C>A
NM_032427.4:c.513+82418C>A MANE Select NP_115803.1:n.513+82418C>A
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