Canonical Allele Identifier: CA403381259
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090708-T-C
MyVariant Identifiers: chr19:g.4090706T>C (hg19) chr19:g.4090708T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090708T>C , CM000681.2:g.4090708T>C GRCh38
NC_000019.9:g.4090706T>C , CM000681.1:g.4090706T>C GRCh37
NC_000019.8:g.4041706T>C NCBI36
NG_007996.1:g.38421A>G , LRG_750:g.38421A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532A>G
ENST00000688002.1:n.3244A>G
ENST00000688751.1:n.229A>G
ENST00000689792.1:n.997A>G
ENST00000262948.10:c.1093A>G MANE Select ENSP00000262948.4:p.Asn365Asp
ENST00000262948.9:c.1093A>G ENSP00000262948.3:p.Asn365Asp
ENST00000394867.8:c.802A>G ENSP00000378336.1:p.Asn268Asp
ENST00000597263.5:n.278A>G
ENST00000599021.1:c.203A>G
ENST00000600584.5:n.2542A>G
ENST00000601786.5:n.1394A>G
NM_030662.3:c.1093A>G , LRG_750t1:c.1093A>G NP_109587.1:p.Asn365Asp
XM_006722799.2:c.814A>G XP_006722862.1:p.Asn272Asp
XM_011528133.1:c.523A>G XP_011526435.1:p.Asn175Asp
NM_030662.4:c.1093A>G MANE Select NP_109587.1:p.Asn365Asp
Search 100 bp 5'
Search 100 bp 3'