Canonical Allele Identifier: CA2360017138
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824285G= , CM000682.2:g.31824285G= GRCh38
NC_000020.10:g.30412088G= , CM000682.1:g.30412088G= GRCh37
NC_000020.9:g.29875749G= NCBI36
NG_012847.1:g.9911G= , LRG_392:g.9911G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.905G= MANE Select ENSP00000365152.4:p.Cys302=
ENST00000375985.4:c.905G= ENSP00000365152.4:p.Cys302=
ENST00000375994.6:c.905G= ENSP00000365162.2:p.Cys302=
NM_033118.3:c.905G= , LRG_392t1:c.905G= NP_149109.1:p.Cys302=
XR_244155.1:n.1271G=
NM_033118.4:c.905G= MANE Select NP_149109.1:p.Cys302=