Canonical Allele Identifier: CA2816132784
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820120C>G , CM000682.2:g.31820120C>G GRCh38
NC_000020.10:g.30407923C>G , CM000682.1:g.30407923C>G GRCh37
NC_000020.9:g.29871584C>G NCBI36
NG_012847.1:g.5746C>G , LRG_392:g.5746C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.53-6C>G MANE Select ENSP00000365152.4:n.53-6C>G
ENST00000375985.4:c.53-6C>G ENSP00000365152.4:n.53-6C>G
ENST00000375994.6:c.53-6C>G ENSP00000365162.2:n.53-6C>G
NM_033118.3:c.53-6C>G , LRG_392t1:c.53-6C>G NP_149109.1:n.53-6C>G
XR_244155.1:n.218-6C>G
NM_033118.4:c.53-6C>G MANE Select NP_149109.1:n.53-6C>G