Canonical Allele Identifier: CA2360015443
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820264G= , CM000682.2:g.31820264G= GRCh38
NC_000020.10:g.30408067G= , CM000682.1:g.30408067G= GRCh37
NC_000020.9:g.29871728G= NCBI36
NG_012847.1:g.5890G= , LRG_392:g.5890G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.191G= MANE Select ENSP00000365152.4:p.Gly64=
ENST00000375985.4:c.191G= ENSP00000365152.4:p.Gly64=
ENST00000375994.6:c.191G= ENSP00000365162.2:p.Gly64=
NM_033118.3:c.191G= , LRG_392t1:c.191G= NP_149109.1:p.Gly64=
XR_244155.1:n.356G=
NM_033118.4:c.191G= MANE Select NP_149109.1:p.Gly64=