Canonical Allele Identifier: CA226636353
Gene: MAML2 HGNC NCBI

Linked Data

dbSNP Id: rs756607844

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.96133439A>C , CM000673.2:g.96133439A>C GRCh38
NC_000011.9:g.95866603A>C , CM000673.1:g.95866603A>C GRCh37
NC_000011.8:g.95506251A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524717.6:c.514-39922T>G MANE Select ENSP00000434552.1:n.514-39922T>G
ENST00000524717.5:c.514-39922T>G ENSP00000434552.1:n.514-39922T>G
NM_032427.3:c.514-39922T>G NP_115803.1:n.514-39922T>G
XM_011543023.1:c.73-39922T>G XP_011541325.1:n.73-39922T>G
XM_011543024.1:c.-171-39922T>G XP_011541326.1:n.-171-39922T>G
XM_011543025.1:c.514-39922T>G XP_011541327.1:n.514-39922T>G
XM_011543023.3:c.73-39922T>G XP_011541325.1:n.73-39922T>G
XM_011543024.3:c.-171-39922T>G XP_011541326.1:n.-171-39922T>G
XM_011543025.2:c.514-39922T>G XP_011541327.1:n.514-39922T>G
NM_032427.4:c.514-39922T>G MANE Select NP_115803.1:n.514-39922T>G