Canonical Allele Identifier: CA882241836

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1476337121
• gnomAD v3: 19-4094635-G-A
• gnomAD v4: 19-4094635-G-A
• MyVariant Identifiers: chr19:g.4094633G>A (hg19) ; chr19:g.4094635G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094635G>A , CM000681.2:g.4094635G>A	GRCh38
NC_000019.9:g.4094633G>A , CM000681.1:g.4094633G>A	GRCh37
NC_000019.8:g.4045633G>A	NCBI36
NG_007996.1:g.34494C>T , LRG_750:g.34494C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-137C>T
ENST00000688002.1:n.3198-137C>T
ENST00000688751.1:n.183-137C>T
ENST00000689792.1:n.951-137C>T
ENST00000262948.10:c.1047-137C>T MANE Select	ENSP00000262948.4:n.1047-137C>T
ENST00000262948.9:c.1047-137C>T	ENSP00000262948.3:n.1047-137C>T
ENST00000394867.8:c.756-137C>T	ENSP00000378336.1:n.756-137C>T
ENST00000597263.5:n.232-137C>T
ENST00000599021.1:c.157-137C>T
ENST00000600584.5:n.2359C>T
ENST00000601786.5:n.1348-137C>T
NM_030662.3:c.1047-137C>T , LRG_750t1:c.1047-137C>T	NP_109587.1:n.1047-137C>T
XM_006722799.2:c.768-137C>T	XP_006722862.1:n.768-137C>T
XM_011528133.1:c.477-137C>T	XP_011526435.1:n.477-137C>T
XM_017026989.1:c.1458C>T	XP_016882478.1:p.Leu486=
XM_017026990.1:c.1179C>T	XP_016882479.1:p.Leu393=
NM_030662.4:c.1047-137C>T MANE Select	NP_109587.1:n.1047-137C>T