Canonical Allele Identifier: CA504984333
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090658-G-C
MyVariant Identifiers: chr19:g.4090656G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090658G>C , CM000681.2:g.4090658G>C GRCh38
NC_000019.9:g.4090656G>C , CM000681.1:g.4090656G>C GRCh37
NC_000019.8:g.4041656G>C NCBI36
NG_007996.1:g.38471C>G , LRG_750:g.38471C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1582C>G
ENST00000688002.1:n.3294C>G
ENST00000688751.1:n.279C>G
ENST00000689792.1:n.1047C>G
ENST00000262948.10:c.1143C>G MANE Select ENSP00000262948.4:p.Gly381=
ENST00000262948.9:c.1143C>G ENSP00000262948.3:p.Gly381=
ENST00000394867.8:c.852C>G ENSP00000378336.1:p.Gly284=
ENST00000597263.5:n.328C>G
ENST00000599021.1:c.253C>G
ENST00000600584.5:n.2592C>G
ENST00000601786.5:n.1444C>G
NM_030662.3:c.1143C>G , LRG_750t1:c.1143C>G NP_109587.1:p.Gly381=
XM_006722799.2:c.864C>G XP_006722862.1:p.Gly288=
XM_011528133.1:c.573C>G XP_011526435.1:p.Gly191=
NM_030662.4:c.1143C>G MANE Select NP_109587.1:p.Gly381=
Search 100 bp 5'
Search 100 bp 3'