Canonical Allele Identifier: CA2360015424
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820216C= , CM000682.2:g.31820216C= GRCh38
NC_000020.10:g.30408019C= , CM000682.1:g.30408019C= GRCh37
NC_000020.9:g.29871680C= NCBI36
NG_012847.1:g.5842C= , LRG_392:g.5842C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.143C= MANE Select ENSP00000365152.4:p.Pro48=
ENST00000375985.4:c.143C= ENSP00000365152.4:p.Pro48=
ENST00000375994.6:c.143C= ENSP00000365162.2:p.Pro48=
NM_033118.3:c.143C= , LRG_392t1:c.143C= NP_149109.1:p.Pro48=
XR_244155.1:n.308C=
NM_033118.4:c.143C= MANE Select NP_149109.1:p.Pro48=