Canonical Allele Identifier: CA9802836
Gene: MYLK2 HGNC NCBI

Linked Data

dbSNP Id: rs765105352

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820150G>A , CM000682.2:g.31820150G>A GRCh38
NC_000020.10:g.30407953G>A , CM000682.1:g.30407953G>A GRCh37
NC_000020.9:g.29871614G>A NCBI36
NG_012847.1:g.5776G>A , LRG_392:g.5776G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.77G>A MANE Select ENSP00000365152.4:p.Gly26Asp
ENST00000375985.4:c.77G>A ENSP00000365152.4:p.Gly26Asp
ENST00000375994.6:c.77G>A ENSP00000365162.2:p.Gly26Asp
NM_033118.3:c.77G>A , LRG_392t1:c.77G>A NP_149109.1:p.Gly26Asp
XR_244155.1:n.242G>A
NM_033118.4:c.77G>A MANE Select NP_149109.1:p.Gly26Asp