Canonical Allele Identifier: CA2360015350
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820069G= , CM000682.2:g.31820069G= GRCh38
NC_000020.10:g.30407872G= , CM000682.1:g.30407872G= GRCh37
NC_000020.9:g.29871533G= NCBI36
NG_012847.1:g.5695G= , LRG_392:g.5695G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.53-57G= MANE Select ENSP00000365152.4:n.53-57G=
ENST00000375985.4:c.53-57G= ENSP00000365152.4:n.53-57G=
ENST00000375994.6:c.53-57G= ENSP00000365162.2:n.53-57G=
NM_033118.3:c.53-57G= , LRG_392t1:c.53-57G= NP_149109.1:n.53-57G=
XR_244155.1:n.218-57G=
NM_033118.4:c.53-57G= MANE Select NP_149109.1:n.53-57G=