Canonical Allele Identifier: CA2123414153

Gene: MYH6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23393708T= , CM000676.2:g.23393708T=	GRCh38
NC_000014.8:g.23862917T= , CM000676.1:g.23862917T=	GRCh37
NC_000014.7:g.22932757T=	NCBI36
NG_023444.1:g.19570A= , LRG_389:g.19570A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405093.9:c.2886A= MANE Select	ENSP00000386041.3:p.Thr962=
ENST00000356287.3:c.2886A=	ENSP00000348634.3:p.Thr962=
ENST00000405093.7:c.2886A=	ENSP00000386041.3:p.Thr962=
NM_002471.3:c.2886A= , LRG_389t1:c.2886A=	NP_002462.2:p.Thr962=
NM_002471.4:c.2886A= MANE Select	NP_002462.2:p.Thr962=