Canonical Allele Identifier: CA403380723
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090621C>G (hg19) chr19:g.4090623C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090623C>G , CM000681.2:g.4090623C>G GRCh38
NC_000019.9:g.4090621C>G , CM000681.1:g.4090621C>G GRCh37
NC_000019.8:g.4041621C>G NCBI36
NG_007996.1:g.38506G>C , LRG_750:g.38506G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1617G>C
ENST00000688002.1:n.3329G>C
ENST00000688751.1:n.314G>C
ENST00000689792.1:n.1082G>C
ENST00000262948.10:c.1178G>C MANE Select ENSP00000262948.4:p.Gly393Ala
ENST00000262948.9:c.1178G>C ENSP00000262948.3:p.Gly393Ala
ENST00000394867.8:c.887G>C ENSP00000378336.1:p.Gly296Ala
ENST00000597263.5:n.363G>C
ENST00000599021.1:c.288G>C
ENST00000600584.5:n.2627G>C
ENST00000601786.5:n.1479G>C
NM_030662.3:c.1178G>C , LRG_750t1:c.1178G>C NP_109587.1:p.Gly393Ala
XM_006722799.2:c.899G>C XP_006722862.1:p.Gly300Ala
XM_011528133.1:c.608G>C XP_011526435.1:p.Gly203Ala
NM_030662.4:c.1178G>C MANE Select NP_109587.1:p.Gly393Ala
Search 100 bp 5'
Search 100 bp 3'