Canonical Allele Identifier: CA403381201
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090696A>C (hg19) chr19:g.4090698A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090698A>C , CM000681.2:g.4090698A>C GRCh38
NC_000019.9:g.4090696A>C , CM000681.1:g.4090696A>C GRCh37
NC_000019.8:g.4041696A>C NCBI36
NG_007996.1:g.38431T>G , LRG_750:g.38431T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1542T>G
ENST00000688002.1:n.3254T>G
ENST00000688751.1:n.239T>G
ENST00000689792.1:n.1007T>G
ENST00000262948.10:c.1103T>G MANE Select ENSP00000262948.4:p.Phe368Cys
ENST00000262948.9:c.1103T>G ENSP00000262948.3:p.Phe368Cys
ENST00000394867.8:c.812T>G ENSP00000378336.1:p.Phe271Cys
ENST00000597263.5:n.288T>G
ENST00000599021.1:c.213T>G
ENST00000600584.5:n.2552T>G
ENST00000601786.5:n.1404T>G
NM_030662.3:c.1103T>G , LRG_750t1:c.1103T>G NP_109587.1:p.Phe368Cys
XM_006722799.2:c.824T>G XP_006722862.1:p.Phe275Cys
XM_011528133.1:c.533T>G XP_011526435.1:p.Phe178Cys
NM_030662.4:c.1103T>G MANE Select NP_109587.1:p.Phe368Cys
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