Canonical Allele Identifier: CA403381138
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090689-C-G
MyVariant Identifiers: chr19:g.4090687C>G (hg19) chr19:g.4090689C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090689C>G , CM000681.2:g.4090689C>G GRCh38
NC_000019.9:g.4090687C>G , CM000681.1:g.4090687C>G GRCh37
NC_000019.8:g.4041687C>G NCBI36
NG_007996.1:g.38440G>C , LRG_750:g.38440G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1551G>C
ENST00000688002.1:n.3263G>C
ENST00000688751.1:n.248G>C
ENST00000689792.1:n.1016G>C
ENST00000262948.10:c.1112G>C MANE Select ENSP00000262948.4:p.Arg371Pro
ENST00000262948.9:c.1112G>C ENSP00000262948.3:p.Arg371Pro
ENST00000394867.8:c.821G>C ENSP00000378336.1:p.Arg274Pro
ENST00000597263.5:n.297G>C
ENST00000599021.1:c.222G>C
ENST00000600584.5:n.2561G>C
ENST00000601786.5:n.1413G>C
NM_030662.3:c.1112G>C , LRG_750t1:c.1112G>C NP_109587.1:p.Arg371Pro
XM_006722799.2:c.833G>C XP_006722862.1:p.Arg278Pro
XM_011528133.1:c.542G>C XP_011526435.1:p.Arg181Pro
NM_030662.4:c.1112G>C MANE Select NP_109587.1:p.Arg371Pro
Search 100 bp 5'
Search 100 bp 3'