Canonical Allele Identifier: CA408524856
Gene: MYLK2 HGNC NCBI

Linked Data

dbSNP Id: rs1157509610
MyVariant Identifiers: chr20:g.30407943G>C (hg19) chr20:g.31820140G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820140G>C , CM000682.2:g.31820140G>C GRCh38
NC_000020.10:g.30407943G>C , CM000682.1:g.30407943G>C GRCh37
NC_000020.9:g.29871604G>C NCBI36
NG_012847.1:g.5766G>C , LRG_392:g.5766G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.67G>C MANE Select ENSP00000365152.4:p.Gly23Arg
ENST00000375985.4:c.67G>C ENSP00000365152.4:p.Gly23Arg
ENST00000375994.6:c.67G>C ENSP00000365162.2:p.Gly23Arg
NM_033118.3:c.67G>C , LRG_392t1:c.67G>C NP_149109.1:p.Gly23Arg
XR_244155.1:n.232G>C
NM_033118.4:c.67G>C MANE Select NP_149109.1:p.Gly23Arg
Search 100 bp 5'
Search 100 bp 3'