Canonical Allele Identifier: CA1993195847
Gene: MAML2 HGNC NCBI

Linked Data

dbSNP Id: rs1362238887
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.96133679G>T , CM000673.2:g.96133679G>T GRCh38
NC_000011.9:g.95866843G>T , CM000673.1:g.95866843G>T GRCh37
NC_000011.8:g.95506491G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524717.6:c.514-40162C>A MANE Select ENSP00000434552.1:n.514-40162C>A
ENST00000524717.5:c.514-40162C>A ENSP00000434552.1:n.514-40162C>A
NM_032427.3:c.514-40162C>A NP_115803.1:n.514-40162C>A
XM_011543023.1:c.73-40162C>A XP_011541325.1:n.73-40162C>A
XM_011543024.1:c.-171-40162C>A XP_011541326.1:n.-171-40162C>A
XM_011543025.1:c.514-40162C>A XP_011541327.1:n.514-40162C>A
XM_011543023.3:c.73-40162C>A XP_011541325.1:n.73-40162C>A
XM_011543024.3:c.-171-40162C>A XP_011541326.1:n.-171-40162C>A
XM_011543025.2:c.514-40162C>A XP_011541327.1:n.514-40162C>A
NM_032427.4:c.514-40162C>A MANE Select NP_115803.1:n.514-40162C>A
Search 100 bp 5'
Search 100 bp 3'