Canonical Allele Identifier: CA2724877350

Gene: MAML2

Linked Data

• dbSNP Id: rs2135858391

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.96133653T>C , CM000673.2:g.96133653T>C	GRCh38
NC_000011.9:g.95866817T>C , CM000673.1:g.95866817T>C	GRCh37
NC_000011.8:g.95506465T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000524717.6:c.514-40136A>G MANE Select	ENSP00000434552.1:n.514-40136A>G
ENST00000524717.5:c.514-40136A>G	ENSP00000434552.1:n.514-40136A>G
NM_032427.3:c.514-40136A>G	NP_115803.1:n.514-40136A>G
XM_011543023.1:c.73-40136A>G	XP_011541325.1:n.73-40136A>G
XM_011543024.1:c.-171-40136A>G	XP_011541326.1:n.-171-40136A>G
XM_011543025.1:c.514-40136A>G	XP_011541327.1:n.514-40136A>G
XM_011543023.3:c.73-40136A>G	XP_011541325.1:n.73-40136A>G
XM_011543024.3:c.-171-40136A>G	XP_011541326.1:n.-171-40136A>G
XM_011543025.2:c.514-40136A>G	XP_011541327.1:n.514-40136A>G
NM_032427.4:c.514-40136A>G MANE Select	NP_115803.1:n.514-40136A>G