Canonical Allele Identifier: CA504984289
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090597C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090599C>T , CM000681.2:g.4090599C>T GRCh38
NC_000019.9:g.4090597C>T , CM000681.1:g.4090597C>T GRCh37
NC_000019.8:g.4041597C>T NCBI36
NG_007996.1:g.38530G>A , LRG_750:g.38530G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1641G>A
ENST00000688002.1:n.3353G>A
ENST00000688751.1:n.338G>A
ENST00000689792.1:n.1106G>A
ENST00000262948.10:c.1202G>A MANE Select ENSP00000262948.4:p.Ter401=
ENST00000262948.9:c.1202G>A ENSP00000262948.3:p.Ter401=
ENST00000394867.8:c.911G>A ENSP00000378336.1:p.Ter304=
ENST00000597263.5:n.387G>A
ENST00000599021.1:c.312G>A
ENST00000600584.5:n.2651G>A
ENST00000601786.5:n.1503G>A
NM_030662.3:c.1202G>A , LRG_750t1:c.1202G>A NP_109587.1:p.Ter401=
XM_006722799.2:c.923G>A XP_006722862.1:p.Ter308=
XM_011528133.1:c.632G>A XP_011526435.1:p.Ter211=
NM_030662.4:c.1202G>A MANE Select NP_109587.1:p.Ter401=
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