Canonical Allele Identifier: CA408526646
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824284T>G , CM000682.2:g.31824284T>G GRCh38
NC_000020.10:g.30412087T>G , CM000682.1:g.30412087T>G GRCh37
NC_000020.9:g.29875748T>G NCBI36
NG_012847.1:g.9910T>G , LRG_392:g.9910T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.904T>G MANE Select ENSP00000365152.4:p.Cys302Gly
ENST00000375985.4:c.904T>G ENSP00000365152.4:p.Cys302Gly
ENST00000375994.6:c.904T>G ENSP00000365162.2:p.Cys302Gly
NM_033118.3:c.904T>G , LRG_392t1:c.904T>G NP_149109.1:p.Cys302Gly
XR_244155.1:n.1270T>G
NM_033118.4:c.904T>G MANE Select NP_149109.1:p.Cys302Gly