Canonical Allele Identifier: CA408525022
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820224A>C , CM000682.2:g.31820224A>C GRCh38
NC_000020.10:g.30408027A>C , CM000682.1:g.30408027A>C GRCh37
NC_000020.9:g.29871688A>C NCBI36
NG_012847.1:g.5850A>C , LRG_392:g.5850A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.151A>C MANE Select ENSP00000365152.4:p.Lys51Gln
ENST00000375985.4:c.151A>C ENSP00000365152.4:p.Lys51Gln
ENST00000375994.6:c.151A>C ENSP00000365162.2:p.Lys51Gln
NM_033118.3:c.151A>C , LRG_392t1:c.151A>C NP_149109.1:p.Lys51Gln
XR_244155.1:n.316A>C
NM_033118.4:c.151A>C MANE Select NP_149109.1:p.Lys51Gln