Canonical Allele Identifier: CA403381231

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4090701G>C (hg19) ; chr19:g.4090703G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090703G>C , CM000681.2:g.4090703G>C	GRCh38
NC_000019.9:g.4090701G>C , CM000681.1:g.4090701G>C	GRCh37
NC_000019.8:g.4041701G>C	NCBI36
NG_007996.1:g.38426C>G , LRG_750:g.38426C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1537C>G
ENST00000688002.1:n.3249C>G
ENST00000688751.1:n.234C>G
ENST00000689792.1:n.1002C>G
ENST00000262948.10:c.1098C>G MANE Select	ENSP00000262948.4:p.His366Gln
ENST00000262948.9:c.1098C>G	ENSP00000262948.3:p.His366Gln
ENST00000394867.8:c.807C>G	ENSP00000378336.1:p.His269Gln
ENST00000597263.5:n.283C>G
ENST00000599021.1:c.208C>G
ENST00000600584.5:n.2547C>G
ENST00000601786.5:n.1399C>G
NM_030662.3:c.1098C>G , LRG_750t1:c.1098C>G	NP_109587.1:p.His366Gln
XM_006722799.2:c.819C>G	XP_006722862.1:p.His273Gln
XM_011528133.1:c.528C>G	XP_011526435.1:p.His176Gln
NM_030662.4:c.1098C>G MANE Select	NP_109587.1:p.His366Gln