Canonical Allele Identifier: CA2360015444

Gene: MYLK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.31820266A= , CM000682.2:g.31820266A=	GRCh38
NC_000020.10:g.30408069A= , CM000682.1:g.30408069A=	GRCh37
NC_000020.9:g.29871730A=	NCBI36
NG_012847.1:g.5892A= , LRG_392:g.5892A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375985.5:c.193A= MANE Select	ENSP00000365152.4:p.Thr65=
ENST00000375985.4:c.193A=	ENSP00000365152.4:p.Thr65=
ENST00000375994.6:c.193A=	ENSP00000365162.2:p.Thr65=
NM_033118.3:c.193A= , LRG_392t1:c.193A=	NP_149109.1:p.Thr65=
XR_244155.1:n.358A=
NM_033118.4:c.193A= MANE Select	NP_149109.1:p.Thr65=