Canonical Allele Identifier: CA408524829
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820126A>T , CM000682.2:g.31820126A>T GRCh38
NC_000020.10:g.30407929A>T , CM000682.1:g.30407929A>T GRCh37
NC_000020.9:g.29871590A>T NCBI36
NG_012847.1:g.5752A>T , LRG_392:g.5752A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.53A>T MANE Select ENSP00000365152.4:p.Asp18Val
ENST00000375985.4:c.53A>T ENSP00000365152.4:p.Asp18Val
ENST00000375994.6:c.53A>T ENSP00000365162.2:p.Asp18Val
NM_033118.3:c.53A>T , LRG_392t1:c.53A>T NP_149109.1:p.Asp18Val
XR_244155.1:n.218A>T
NM_033118.4:c.53A>T MANE Select NP_149109.1:p.Asp18Val