Canonical Allele Identifier: CA408526664
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30412094A>T (hg19) chr20:g.31824291A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824291A>T , CM000682.2:g.31824291A>T GRCh38
NC_000020.10:g.30412094A>T , CM000682.1:g.30412094A>T GRCh37
NC_000020.9:g.29875755A>T NCBI36
NG_012847.1:g.9917A>T , LRG_392:g.9917A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.911A>T MANE Select ENSP00000365152.4:p.Glu304Val
ENST00000375985.4:c.911A>T ENSP00000365152.4:p.Glu304Val
ENST00000375994.6:c.911A>T ENSP00000365162.2:p.Glu304Val
NM_033118.3:c.911A>T , LRG_392t1:c.911A>T NP_149109.1:p.Glu304Val
XR_244155.1:n.1277A>T
NM_033118.4:c.911A>T MANE Select NP_149109.1:p.Glu304Val
Search 100 bp 5'
Search 100 bp 3'