Canonical Allele Identifier: CA408524849
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820137A>G , CM000682.2:g.31820137A>G GRCh38
NC_000020.10:g.30407940A>G , CM000682.1:g.30407940A>G GRCh37
NC_000020.9:g.29871601A>G NCBI36
NG_012847.1:g.5763A>G , LRG_392:g.5763A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.64A>G MANE Select ENSP00000365152.4:p.Lys22Glu
ENST00000375985.4:c.64A>G ENSP00000365152.4:p.Lys22Glu
ENST00000375994.6:c.64A>G ENSP00000365162.2:p.Lys22Glu
NM_033118.3:c.64A>G , LRG_392t1:c.64A>G NP_149109.1:p.Lys22Glu
XR_244155.1:n.229A>G
NM_033118.4:c.64A>G MANE Select NP_149109.1:p.Lys22Glu