Canonical Allele Identifier: CA510174083
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30408053A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820250A>C , CM000682.2:g.31820250A>C GRCh38
NC_000020.10:g.30408053A>C , CM000682.1:g.30408053A>C GRCh37
NC_000020.9:g.29871714A>C NCBI36
NG_012847.1:g.5876A>C , LRG_392:g.5876A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.177A>C MANE Select ENSP00000365152.4:p.Ser59=
ENST00000375985.4:c.177A>C ENSP00000365152.4:p.Ser59=
ENST00000375994.6:c.177A>C ENSP00000365162.2:p.Ser59=
NM_033118.3:c.177A>C , LRG_392t1:c.177A>C NP_149109.1:p.Ser59=
XR_244155.1:n.342A>C
NM_033118.4:c.177A>C MANE Select NP_149109.1:p.Ser59=
Search 100 bp 5'
Search 100 bp 3'