Canonical Allele Identifier: CA2360015445
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820267C= , CM000682.2:g.31820267C= GRCh38
NC_000020.10:g.30408070C= , CM000682.1:g.30408070C= GRCh37
NC_000020.9:g.29871731C= NCBI36
NG_012847.1:g.5893C= , LRG_392:g.5893C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.194C= MANE Select ENSP00000365152.4:p.Thr65=
ENST00000375985.4:c.194C= ENSP00000365152.4:p.Thr65=
ENST00000375994.6:c.194C= ENSP00000365162.2:p.Thr65=
NM_033118.3:c.194C= , LRG_392t1:c.194C= NP_149109.1:p.Thr65=
XR_244155.1:n.359C=
NM_033118.4:c.194C= MANE Select NP_149109.1:p.Thr65=