Canonical Allele Identifier: CA408524877
Gene: MYLK2 HGNC NCBI

Linked Data

COSMIC: COSM1713315
MyVariant Identifiers: chr20:g.30407955G>A (hg19) chr20:g.31820152G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820152G>A , CM000682.2:g.31820152G>A GRCh38
NC_000020.10:g.30407955G>A , CM000682.1:g.30407955G>A GRCh37
NC_000020.9:g.29871616G>A NCBI36
NG_012847.1:g.5778G>A , LRG_392:g.5778G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.79G>A MANE Select ENSP00000365152.4:p.Glu27Lys
ENST00000375985.4:c.79G>A ENSP00000365152.4:p.Glu27Lys
ENST00000375994.6:c.79G>A ENSP00000365162.2:p.Glu27Lys
NM_033118.3:c.79G>A , LRG_392t1:c.79G>A NP_149109.1:p.Glu27Lys
XR_244155.1:n.244G>A
NM_033118.4:c.79G>A MANE Select NP_149109.1:p.Glu27Lys
Search 100 bp 5'
Search 100 bp 3'