Canonical Allele Identifier: CA403392457

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2041237436
• gnomAD v4: 19-4117451-G-A
• MyVariant Identifiers: chr19:g.4117449G>A (hg19) ; chr19:g.4117451G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117451G>A , CM000681.2:g.4117451G>A	GRCh38
NC_000019.9:g.4117449G>A , CM000681.1:g.4117449G>A	GRCh37
NC_000019.8:g.4068449G>A	NCBI36
NG_007996.1:g.11678C>T , LRG_750:g.11678C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.710C>T
ENST00000687128.1:n.710C>T
ENST00000262948.10:c.271C>T MANE Select	ENSP00000262948.4:p.His91Tyr
ENST00000262948.9:c.271C>T	ENSP00000262948.3:p.His91Tyr
ENST00000394867.8:c.-21C>T	ENSP00000378336.1:n.-21C>T
ENST00000599345.1:n.468C>T
NM_030662.3:c.271C>T , LRG_750t1:c.271C>T	NP_109587.1:p.His91Tyr
XM_006722799.2:c.271C>T	XP_006722862.1:p.His91Tyr
XM_017026989.1:c.271C>T	XP_016882478.1:p.His91Tyr
XM_017026990.1:c.271C>T	XP_016882479.1:p.His91Tyr
XM_017026991.1:c.271C>T	XP_016882480.1:p.His91Tyr
NM_030662.4:c.271C>T MANE Select	NP_109587.1:p.His91Tyr