Canonical Allele Identifier: CA304449375

Gene: MAP2K2

Linked Data

• dbSNP Id: rs757052152
• gnomAD v2: 19-4099553-T-C
• gnomAD v3: 19-4099555-T-C
• gnomAD v4: 19-4099555-T-C
• MyVariant Identifiers: chr19:g.4099553T>C (hg19) ; chr19:g.4099555T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099555T>C , CM000681.2:g.4099555T>C	GRCh38
NC_000019.9:g.4099553T>C , CM000681.1:g.4099553T>C	GRCh37
NC_000019.8:g.4050553T>C	NCBI36
NG_007996.1:g.29574A>G , LRG_750:g.29574A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-141A>G
ENST00000687128.1:n.1145-141A>G
ENST00000688002.1:n.859A>G
ENST00000689792.1:n.646-177A>G
ENST00000262948.10:c.706-141A>G MANE Select	ENSP00000262948.4:n.706-141A>G
ENST00000262948.9:c.706-141A>G	ENSP00000262948.3:n.706-141A>G
ENST00000394867.8:c.415-141A>G	ENSP00000378336.1:n.415-141A>G
ENST00000593364.5:n.653-141A>G
ENST00000595715.1:n.380A>G
ENST00000597263.5:n.169+1464A>G
ENST00000599021.1:c.29+1464A>G
ENST00000600584.5:n.1125A>G
ENST00000601786.5:n.1007-141A>G
ENST00000602167.5:n.426-141A>G
NM_030662.3:c.706-141A>G , LRG_750t1:c.706-141A>G	NP_109587.1:n.706-141A>G
XM_006722799.2:c.705+1464A>G	XP_006722862.1:n.705+1464A>G
XM_011528133.1:c.136-141A>G	XP_011526435.1:n.136-141A>G
XM_017026989.1:c.706-141A>G	XP_016882478.1:n.706-141A>G
XM_017026990.1:c.705+1464A>G	XP_016882479.1:n.705+1464A>G
XM_017026991.1:c.*175A>G	XP_016882480.1:n.*175A>G
NM_030662.4:c.706-141A>G MANE Select	NP_109587.1:n.706-141A>G