Canonical Allele Identifier: CA2360015378
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820143C= , CM000682.2:g.31820143C= GRCh38
NC_000020.10:g.30407946C= , CM000682.1:g.30407946C= GRCh37
NC_000020.9:g.29871607C= NCBI36
NG_012847.1:g.5769C= , LRG_392:g.5769C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.70C= MANE Select ENSP00000365152.4:p.Pro24=
ENST00000375985.4:c.70C= ENSP00000365152.4:p.Pro24=
ENST00000375994.6:c.70C= ENSP00000365162.2:p.Pro24=
NM_033118.3:c.70C= , LRG_392t1:c.70C= NP_149109.1:p.Pro24=
XR_244155.1:n.235C=
NM_033118.4:c.70C= MANE Select NP_149109.1:p.Pro24=