Canonical Allele Identifier: CA2360015433
Gene: MYLK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820240C= , CM000682.2:g.31820240C= GRCh38
NC_000020.10:g.30408043C= , CM000682.1:g.30408043C= GRCh37
NC_000020.9:g.29871704C= NCBI36
NG_012847.1:g.5866C= , LRG_392:g.5866C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.167C= MANE Select ENSP00000365152.4:p.Ala56=
ENST00000375985.4:c.167C= ENSP00000365152.4:p.Ala56=
ENST00000375994.6:c.167C= ENSP00000365162.2:p.Ala56=
NM_033118.3:c.167C= , LRG_392t1:c.167C= NP_149109.1:p.Ala56=
XR_244155.1:n.332C=
NM_033118.4:c.167C= MANE Select NP_149109.1:p.Ala56=
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