Canonical Allele Identifier: CA1362297091
Gene: MYL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46859506A= , CM000665.2:g.46859506A= GRCh38
NC_000003.11:g.46900996A= , CM000665.1:g.46900996A= GRCh37
NC_000003.10:g.46876000A= NCBI36
NG_007555.2:g.27664T= , LRG_395:g.27664T=

Transcript Alleles

HGVS Amino-acid change
ENST00000431168.2:c.450T= ENSP00000393455.2:p.Gly150=
ENST00000292327.6:c.450T= MANE Select ENSP00000292327.4:p.Gly150=
ENST00000653454.1:c.450T= ENSP00000499624.1:p.Gly150=
ENST00000654597.1:c.450T= ENSP00000499406.1:p.Gly150=
ENST00000655244.1:n.672T=
ENST00000662933.1:c.450T= ENSP00000499577.1:p.Gly150=
ENST00000664891.1:n.408T=
ENST00000292327.4:c.450T= ENSP00000292327.4:p.Gly150=
ENST00000395869.5:c.450T= ENSP00000379210.1:p.Gly150=
NM_000258.2:c.450T= , LRG_395t1:c.450T= NP_000249.1:p.Gly150=
NM_000258.3:c.450T= MANE Select NP_000249.1:p.Gly150=