Canonical Allele Identifier: CA408524902
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30407967G>A (hg19) chr20:g.31820164G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820164G>A , CM000682.2:g.31820164G>A GRCh38
NC_000020.10:g.30407967G>A , CM000682.1:g.30407967G>A GRCh37
NC_000020.9:g.29871628G>A NCBI36
NG_012847.1:g.5790G>A , LRG_392:g.5790G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.91G>A MANE Select ENSP00000365152.4:p.Ala31Thr
ENST00000375985.4:c.91G>A ENSP00000365152.4:p.Ala31Thr
ENST00000375994.6:c.91G>A ENSP00000365162.2:p.Ala31Thr
NM_033118.3:c.91G>A , LRG_392t1:c.91G>A NP_149109.1:p.Ala31Thr
XR_244155.1:n.256G>A
NM_033118.4:c.91G>A MANE Select NP_149109.1:p.Ala31Thr
Search 100 bp 5'
Search 100 bp 3'