Canonical Allele Identifier: CA2360015440
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820258G= , CM000682.2:g.31820258G= GRCh38
NC_000020.10:g.30408061G= , CM000682.1:g.30408061G= GRCh37
NC_000020.9:g.29871722G= NCBI36
NG_012847.1:g.5884G= , LRG_392:g.5884G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.185G= MANE Select ENSP00000365152.4:p.Gly62=
ENST00000375985.4:c.185G= ENSP00000365152.4:p.Gly62=
ENST00000375994.6:c.185G= ENSP00000365162.2:p.Gly62=
NM_033118.3:c.185G= , LRG_392t1:c.185G= NP_149109.1:p.Gly62=
XR_244155.1:n.350G=
NM_033118.4:c.185G= MANE Select NP_149109.1:p.Gly62=