Canonical Allele Identifier: CA2360015394
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820165C= , CM000682.2:g.31820165C= GRCh38
NC_000020.10:g.30407968C= , CM000682.1:g.30407968C= GRCh37
NC_000020.9:g.29871629C= NCBI36
NG_012847.1:g.5791C= , LRG_392:g.5791C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.92C= MANE Select ENSP00000365152.4:p.Ala31=
ENST00000375985.4:c.92C= ENSP00000365152.4:p.Ala31=
ENST00000375994.6:c.92C= ENSP00000365162.2:p.Ala31=
NM_033118.3:c.92C= , LRG_392t1:c.92C= NP_149109.1:p.Ala31=
XR_244155.1:n.257C=
NM_033118.4:c.92C= MANE Select NP_149109.1:p.Ala31=