Canonical Allele Identifier: CA408526652
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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