Canonical Allele Identifier: CA13393378
Gene: MAML2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10765792

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.96133536G>C , CM000673.2:g.96133536G>C GRCh38
NC_000011.9:g.95866700G>C , CM000673.1:g.95866700G>C GRCh37
NC_000011.8:g.95506348G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_032427.3:c.514-40019C>G VV NP_115803.1:p.=
XM_011543023.1:c.73-40019C>G XP_011541325.1:p.=
XM_011543024.1:c.-171-40019C>G XP_011541326.1:p.=
XM_011543025.1:c.514-40019C>G XP_011541327.1:p.=
XM_011543023.3:c.73-40019C>G
XM_011543024.3:c.-171-40019C>G
XM_011543025.2:c.514-40019C>G
NM_032427.4:c.514-40019C>G VV MANE Preferred
ENST00000524717.5:c.514-40019C>G ENSP00000434552.1:p.=