Canonical Allele Identifier: CA408526658
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30412092G>C (hg19) chr20:g.31824289G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824289G>C , CM000682.2:g.31824289G>C GRCh38
NC_000020.10:g.30412092G>C , CM000682.1:g.30412092G>C GRCh37
NC_000020.9:g.29875753G>C NCBI36
NG_012847.1:g.9915G>C , LRG_392:g.9915G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375985.5:c.909G>C MANE Select ENSP00000365152.4:p.Met303Ile
ENST00000375985.4:c.909G>C ENSP00000365152.4:p.Met303Ile
ENST00000375994.6:c.909G>C ENSP00000365162.2:p.Met303Ile
NM_033118.3:c.909G>C , LRG_392t1:c.909G>C NP_149109.1:p.Met303Ile
XR_244155.1:n.1275G>C
NM_033118.4:c.909G>C MANE Select NP_149109.1:p.Met303Ile
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