Canonical Allele Identifier: CA510174119
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30408071C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820268C>T , CM000682.2:g.31820268C>T GRCh38
NC_000020.10:g.30408071C>T , CM000682.1:g.30408071C>T GRCh37
NC_000020.9:g.29871732C>T NCBI36
NG_012847.1:g.5894C>T , LRG_392:g.5894C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.195C>T MANE Select ENSP00000365152.4:p.Thr65=
ENST00000375985.4:c.195C>T ENSP00000365152.4:p.Thr65=
ENST00000375994.6:c.195C>T ENSP00000365162.2:p.Thr65=
NM_033118.3:c.195C>T , LRG_392t1:c.195C>T NP_149109.1:p.Thr65=
XR_244155.1:n.360C>T
NM_033118.4:c.195C>T MANE Select NP_149109.1:p.Thr65=