Canonical Allele Identifier: CA2360017140
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824290G= , CM000682.2:g.31824290G= GRCh38
NC_000020.10:g.30412093G= , CM000682.1:g.30412093G= GRCh37
NC_000020.9:g.29875754G= NCBI36
NG_012847.1:g.9916G= , LRG_392:g.9916G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.910G= MANE Select ENSP00000365152.4:p.Glu304=
ENST00000375985.4:c.910G= ENSP00000365152.4:p.Glu304=
ENST00000375994.6:c.910G= ENSP00000365162.2:p.Glu304=
NM_033118.3:c.910G= , LRG_392t1:c.910G= NP_149109.1:p.Glu304=
XR_244155.1:n.1276G=
NM_033118.4:c.910G= MANE Select NP_149109.1:p.Glu304=