Canonical Allele Identifier: CA2360015382
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820149G= , CM000682.2:g.31820149G= GRCh38
NC_000020.10:g.30407952G= , CM000682.1:g.30407952G= GRCh37
NC_000020.9:g.29871613G= NCBI36
NG_012847.1:g.5775G= , LRG_392:g.5775G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.76G= MANE Select ENSP00000365152.4:p.Gly26=
ENST00000375985.4:c.76G= ENSP00000365152.4:p.Gly26=
ENST00000375994.6:c.76G= ENSP00000365162.2:p.Gly26=
NM_033118.3:c.76G= , LRG_392t1:c.76G= NP_149109.1:p.Gly26=
XR_244155.1:n.241G=
NM_033118.4:c.76G= MANE Select NP_149109.1:p.Gly26=