Canonical Allele Identifier: CA2360015425
Gene: MYLK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820217C= , CM000682.2:g.31820217C= GRCh38
NC_000020.10:g.30408020C= , CM000682.1:g.30408020C= GRCh37
NC_000020.9:g.29871681C= NCBI36
NG_012847.1:g.5843C= , LRG_392:g.5843C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.144C= MANE Select ENSP00000365152.4:p.Pro48=
ENST00000375985.4:c.144C= ENSP00000365152.4:p.Pro48=
ENST00000375994.6:c.144C= ENSP00000365162.2:p.Pro48=
NM_033118.3:c.144C= , LRG_392t1:c.144C= NP_149109.1:p.Pro48=
XR_244155.1:n.309C=
NM_033118.4:c.144C= MANE Select NP_149109.1:p.Pro48=
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