Canonical Allele Identifier: CA504984358
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090695G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090697G>A , CM000681.2:g.4090697G>A GRCh38
NC_000019.9:g.4090695G>A , CM000681.1:g.4090695G>A GRCh37
NC_000019.8:g.4041695G>A NCBI36
NG_007996.1:g.38432C>T , LRG_750:g.38432C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1543C>T
ENST00000688002.1:n.3255C>T
ENST00000688751.1:n.240C>T
ENST00000689792.1:n.1008C>T
ENST00000262948.10:c.1104C>T MANE Select ENSP00000262948.4:p.Phe368=
ENST00000262948.9:c.1104C>T ENSP00000262948.3:p.Phe368=
ENST00000394867.8:c.813C>T ENSP00000378336.1:p.Phe271=
ENST00000597263.5:n.289C>T
ENST00000599021.1:c.214C>T
ENST00000600584.5:n.2553C>T
ENST00000601786.5:n.1405C>T
NM_030662.3:c.1104C>T , LRG_750t1:c.1104C>T NP_109587.1:p.Phe368=
XM_006722799.2:c.825C>T XP_006722862.1:p.Phe275=
XM_011528133.1:c.534C>T XP_011526435.1:p.Phe178=
NM_030662.4:c.1104C>T MANE Select NP_109587.1:p.Phe368=
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