Canonical Allele Identifier: CA304445575
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs781375177
MyVariant Identifiers: chr19:g.4090409C>G (hg19) chr19:g.4090411C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090411C>G , CM000681.2:g.4090411C>G GRCh38
NC_000019.9:g.4090409C>G , CM000681.1:g.4090409C>G GRCh37
NC_000019.8:g.4041409C>G NCBI36
NG_007996.1:g.38718G>C , LRG_750:g.38718G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1829G>C
ENST00000688751.1:n.526G>C
ENST00000689792.1:n.1294G>C
ENST00000262948.10:c.*187G>C MANE Select ENSP00000262948.4:n.*187G>C
ENST00000262948.9:c.*187G>C ENSP00000262948.3:n.*187G>C
ENST00000394867.8:c.*187G>C ENSP00000378336.1:n.*187G>C
ENST00000600584.5:n.2839G>C
ENST00000601786.5:n.1691G>C
NM_030662.3:c.*187G>C , LRG_750t1:c.*187G>C NP_109587.1:n.*187G>C
XM_006722799.2:c.*187G>C XP_006722862.1:n.*187G>C
XM_011528133.1:c.*187G>C XP_011526435.1:n.*187G>C
NM_030662.4:c.*187G>C MANE Select NP_109587.1:n.*187G>C
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