Canonical Allele Identifier: CA504984338
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090664-A-G
MyVariant Identifiers: chr19:g.4090662A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090664A>G , CM000681.2:g.4090664A>G GRCh38
NC_000019.9:g.4090662A>G , CM000681.1:g.4090662A>G GRCh37
NC_000019.8:g.4041662A>G NCBI36
NG_007996.1:g.38465T>C , LRG_750:g.38465T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1576T>C
ENST00000688002.1:n.3288T>C
ENST00000688751.1:n.273T>C
ENST00000689792.1:n.1041T>C
ENST00000262948.10:c.1137T>C MANE Select ENSP00000262948.4:p.Phe379=
ENST00000262948.9:c.1137T>C ENSP00000262948.3:p.Phe379=
ENST00000394867.8:c.846T>C ENSP00000378336.1:p.Phe282=
ENST00000597263.5:n.322T>C
ENST00000599021.1:c.247T>C
ENST00000600584.5:n.2586T>C
ENST00000601786.5:n.1438T>C
NM_030662.3:c.1137T>C , LRG_750t1:c.1137T>C NP_109587.1:p.Phe379=
XM_006722799.2:c.858T>C XP_006722862.1:p.Phe286=
XM_011528133.1:c.567T>C XP_011526435.1:p.Phe189=
NM_030662.4:c.1137T>C MANE Select NP_109587.1:p.Phe379=