Canonical Allele Identifier: CA2360017139
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824288T= , CM000682.2:g.31824288T= GRCh38
NC_000020.10:g.30412091T= , CM000682.1:g.30412091T= GRCh37
NC_000020.9:g.29875752T= NCBI36
NG_012847.1:g.9914T= , LRG_392:g.9914T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.908T= MANE Select ENSP00000365152.4:p.Met303=
ENST00000375985.4:c.908T= ENSP00000365152.4:p.Met303=
ENST00000375994.6:c.908T= ENSP00000365162.2:p.Met303=
NM_033118.3:c.908T= , LRG_392t1:c.908T= NP_149109.1:p.Met303=
XR_244155.1:n.1274T=
NM_033118.4:c.908T= MANE Select NP_149109.1:p.Met303=