Canonical Allele Identifier: CA408524880
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820153A>G , CM000682.2:g.31820153A>G GRCh38
NC_000020.10:g.30407956A>G , CM000682.1:g.30407956A>G GRCh37
NC_000020.9:g.29871617A>G NCBI36
NG_012847.1:g.5779A>G , LRG_392:g.5779A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.80A>G MANE Select ENSP00000365152.4:p.Glu27Gly
ENST00000375985.4:c.80A>G ENSP00000365152.4:p.Glu27Gly
ENST00000375994.6:c.80A>G ENSP00000365162.2:p.Glu27Gly
NM_033118.3:c.80A>G , LRG_392t1:c.80A>G NP_149109.1:p.Glu27Gly
XR_244155.1:n.245A>G
NM_033118.4:c.80A>G MANE Select NP_149109.1:p.Glu27Gly