Canonical Allele Identifier: CA2319219655
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1041835574
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090467G>C , CM000681.2:g.4090467G>C GRCh38
NC_000019.9:g.4090465G>C , CM000681.1:g.4090465G>C GRCh37
NC_000019.8:g.4041465G>C NCBI36
NG_007996.1:g.38662C>G , LRG_750:g.38662C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1773C>G
ENST00000688002.1:n.3485C>G
ENST00000688751.1:n.470C>G
ENST00000689792.1:n.1238C>G
ENST00000262948.10:c.*131C>G MANE Select ENSP00000262948.4:n.*131C>G
ENST00000262948.9:c.*131C>G ENSP00000262948.3:n.*131C>G
ENST00000394867.8:c.*131C>G ENSP00000378336.1:n.*131C>G
ENST00000597263.5:n.519C>G
ENST00000600584.5:n.2783C>G
ENST00000601786.5:n.1635C>G
NM_030662.3:c.*131C>G , LRG_750t1:c.*131C>G NP_109587.1:n.*131C>G
XM_006722799.2:c.*131C>G XP_006722862.1:n.*131C>G
XM_011528133.1:c.*131C>G XP_011526435.1:n.*131C>G
NM_030662.4:c.*131C>G MANE Select NP_109587.1:n.*131C>G
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