Canonical Allele Identifier: CA2360015368
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820119T= , CM000682.2:g.31820119T= GRCh38
NC_000020.10:g.30407922T= , CM000682.1:g.30407922T= GRCh37
NC_000020.9:g.29871583T= NCBI36
NG_012847.1:g.5745T= , LRG_392:g.5745T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.53-7T= MANE Select ENSP00000365152.4:n.53-7T=
ENST00000375985.4:c.53-7T= ENSP00000365152.4:n.53-7T=
ENST00000375994.6:c.53-7T= ENSP00000365162.2:n.53-7T=
NM_033118.3:c.53-7T= , LRG_392t1:c.53-7T= NP_149109.1:n.53-7T=
XR_244155.1:n.218-7T=
NM_033118.4:c.53-7T= MANE Select NP_149109.1:n.53-7T=