Canonical Allele Identifier: CA882241810
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1269755077

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094211A>G , CM000681.2:g.4094211A>G GRCh38
NC_000019.9:g.4094209A>G , CM000681.1:g.4094209A>G GRCh37
NC_000019.8:g.4045209A>G NCBI36
NG_007996.1:g.34918T>C , LRG_750:g.34918T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1531+242T>C
ENST00000688002.1:n.3243+242T>C
ENST00000688751.1:n.228+242T>C
ENST00000689792.1:n.996+242T>C
ENST00000262948.10:c.1092+242T>C MANE Select ENSP00000262948.4:n.1092+242T>C
ENST00000262948.9:c.1092+242T>C ENSP00000262948.3:n.1092+242T>C
ENST00000394867.8:c.801+242T>C ENSP00000378336.1:n.801+242T>C
ENST00000597263.5:n.277+242T>C
ENST00000599021.1:c.202+242T>C
ENST00000600584.5:n.2541+242T>C
ENST00000601786.5:n.1393+242T>C
NM_030662.3:c.1092+242T>C , LRG_750t1:c.1092+242T>C NP_109587.1:n.1092+242T>C
XM_006722799.2:c.813+242T>C XP_006722862.1:n.813+242T>C
XM_011528133.1:c.522+242T>C XP_011526435.1:n.522+242T>C
NM_030662.4:c.1092+242T>C MANE Select NP_109587.1:n.1092+242T>C