Canonical Allele Identifier: CA2360015406
Gene: MYLK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820180C= , CM000682.2:g.31820180C= GRCh38
NC_000020.10:g.30407983C= , CM000682.1:g.30407983C= GRCh37
NC_000020.9:g.29871644C= NCBI36
NG_012847.1:g.5806C= , LRG_392:g.5806C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.107C= MANE Select ENSP00000365152.4:p.Pro36=
ENST00000375985.4:c.107C= ENSP00000365152.4:p.Pro36=
ENST00000375994.6:c.107C= ENSP00000365162.2:p.Pro36=
NM_033118.3:c.107C= , LRG_392t1:c.107C= NP_149109.1:p.Pro36=
XR_244155.1:n.272C=
NM_033118.4:c.107C= MANE Select NP_149109.1:p.Pro36=
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