Canonical Allele Identifier: CA2585249173
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4110380-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4110380G>C , CM000681.2:g.4110380G>C GRCh38
NC_000019.9:g.4110378G>C , CM000681.1:g.4110378G>C GRCh37
NC_000019.8:g.4061378G>C NCBI36
NG_007996.1:g.18749C>G , LRG_750:g.18749C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.889+129C>G
ENST00000687128.1:n.889+129C>G
ENST00000262948.10:c.450+129C>G MANE Select ENSP00000262948.4:n.450+129C>G
ENST00000262948.9:c.450+129C>G ENSP00000262948.3:n.450+129C>G
ENST00000394867.8:c.159+129C>G ENSP00000378336.1:n.159+129C>G
ENST00000599345.1:n.647+129C>G
NM_030662.3:c.450+129C>G , LRG_750t1:c.450+129C>G NP_109587.1:n.450+129C>G
XM_006722799.2:c.450+129C>G XP_006722862.1:n.450+129C>G
XM_017026989.1:c.450+129C>G XP_016882478.1:n.450+129C>G
XM_017026990.1:c.450+129C>G XP_016882479.1:n.450+129C>G
XM_017026991.1:c.450+129C>G XP_016882480.1:n.450+129C>G
NM_030662.4:c.450+129C>G MANE Select NP_109587.1:n.450+129C>G