Canonical Allele Identifier: CA408526645
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.904T>C MANE Select ENSP00000365152.4:p.Cys302Arg
ENST00000375985.4:c.904T>C ENSP00000365152.4:p.Cys302Arg
ENST00000375994.6:c.904T>C ENSP00000365162.2:p.Cys302Arg
NM_033118.3:c.904T>C , LRG_392t1:c.904T>C NP_149109.1:p.Cys302Arg
XR_244155.1:n.1270T>C
NM_033118.4:c.904T>C MANE Select NP_149109.1:p.Cys302Arg