Canonical Allele Identifier: CA408526654
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824287A>C , CM000682.2:g.31824287A>C GRCh38
NC_000020.10:g.30412090A>C , CM000682.1:g.30412090A>C GRCh37
NC_000020.9:g.29875751A>C NCBI36
NG_012847.1:g.9913A>C , LRG_392:g.9913A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.907A>C MANE Select ENSP00000365152.4:p.Met303Leu
ENST00000375985.4:c.907A>C ENSP00000365152.4:p.Met303Leu
ENST00000375994.6:c.907A>C ENSP00000365162.2:p.Met303Leu
NM_033118.3:c.907A>C , LRG_392t1:c.907A>C NP_149109.1:p.Met303Leu
XR_244155.1:n.1273A>C
NM_033118.4:c.907A>C MANE Select NP_149109.1:p.Met303Leu