Canonical Allele Identifier: CA408526649
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824285G>T , CM000682.2:g.31824285G>T GRCh38
NC_000020.10:g.30412088G>T , CM000682.1:g.30412088G>T GRCh37
NC_000020.9:g.29875749G>T NCBI36
NG_012847.1:g.9911G>T , LRG_392:g.9911G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.905G>T MANE Select ENSP00000365152.4:p.Cys302Phe
ENST00000375985.4:c.905G>T ENSP00000365152.4:p.Cys302Phe
ENST00000375994.6:c.905G>T ENSP00000365162.2:p.Cys302Phe
NM_033118.3:c.905G>T , LRG_392t1:c.905G>T NP_149109.1:p.Cys302Phe
XR_244155.1:n.1271G>T
NM_033118.4:c.905G>T MANE Select NP_149109.1:p.Cys302Phe