Canonical Allele Identifier: CA510174002
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30407984T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820181T>C , CM000682.2:g.31820181T>C GRCh38
NC_000020.10:g.30407984T>C , CM000682.1:g.30407984T>C GRCh37
NC_000020.9:g.29871645T>C NCBI36
NG_012847.1:g.5807T>C , LRG_392:g.5807T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.108T>C MANE Select ENSP00000365152.4:p.Pro36=
ENST00000375985.4:c.108T>C ENSP00000365152.4:p.Pro36=
ENST00000375994.6:c.108T>C ENSP00000365162.2:p.Pro36=
NM_033118.3:c.108T>C , LRG_392t1:c.108T>C NP_149109.1:p.Pro36=
XR_244155.1:n.273T>C
NM_033118.4:c.108T>C MANE Select NP_149109.1:p.Pro36=
Search 100 bp 5'
Search 100 bp 3'