Canonical Allele Identifier: CA408525102
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30408065T>G (hg19) chr20:g.31820262T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820262T>G , CM000682.2:g.31820262T>G GRCh38
NC_000020.10:g.30408065T>G , CM000682.1:g.30408065T>G GRCh37
NC_000020.9:g.29871726T>G NCBI36
NG_012847.1:g.5888T>G , LRG_392:g.5888T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.189T>G MANE Select ENSP00000365152.4:p.Asp63Glu
ENST00000375985.4:c.189T>G ENSP00000365152.4:p.Asp63Glu
ENST00000375994.6:c.189T>G ENSP00000365162.2:p.Asp63Glu
NM_033118.3:c.189T>G , LRG_392t1:c.189T>G NP_149109.1:p.Asp63Glu
XR_244155.1:n.354T>G
NM_033118.4:c.189T>G MANE Select NP_149109.1:p.Asp63Glu
Search 100 bp 5'
Search 100 bp 3'