Canonical Allele Identifier: CA510174120
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30408071C>G (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.195C>G MANE Select ENSP00000365152.4:p.Thr65=
ENST00000375985.4:c.195C>G ENSP00000365152.4:p.Thr65=
ENST00000375994.6:c.195C>G ENSP00000365162.2:p.Thr65=
NM_033118.3:c.195C>G , LRG_392t1:c.195C>G NP_149109.1:p.Thr65=
XR_244155.1:n.360C>G
NM_033118.4:c.195C>G MANE Select NP_149109.1:p.Thr65=
Search 100 bp 5'
Search 100 bp 3'