Canonical Allele Identifier: CA304447574
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs369694857
gnomAD v2: 19-4095471-G-A
gnomAD v3: 19-4095473-G-A
gnomAD v4: 19-4095473-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4095473G>A , CM000681.2:g.4095473G>A GRCh38
NC_000019.9:g.4095471G>A , CM000681.1:g.4095471G>A GRCh37
NC_000019.8:g.4046471G>A NCBI36
NG_007996.1:g.33656C>T , LRG_750:g.33656C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1424-24C>T
ENST00000688002.1:n.3136-24C>T
ENST00000688751.1:n.121-24C>T
ENST00000689792.1:n.889-24C>T
ENST00000262948.10:c.985-24C>T MANE Select ENSP00000262948.4:n.985-24C>T
ENST00000262948.9:c.985-24C>T ENSP00000262948.3:n.985-24C>T
ENST00000394867.8:c.694-24C>T ENSP00000378336.1:n.694-24C>T
ENST00000595715.1:n.800-24C>T
ENST00000597263.5:n.170-24C>T
ENST00000599021.1:c.95-24C>T
ENST00000600584.5:n.1545-24C>T
ENST00000601786.5:n.1286-24C>T
NM_030662.3:c.985-24C>T , LRG_750t1:c.985-24C>T NP_109587.1:n.985-24C>T
XM_006722799.2:c.706-24C>T XP_006722862.1:n.706-24C>T
XM_011528133.1:c.415-24C>T XP_011526435.1:n.415-24C>T
XM_017026989.1:c.985-24C>T XP_016882478.1:n.985-24C>T
XM_017026990.1:c.706-24C>T XP_016882479.1:n.706-24C>T
NM_030662.4:c.985-24C>T MANE Select NP_109587.1:n.985-24C>T