Canonical Allele Identifier: CA2123414041

Gene: MYH6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23393636T= , CM000676.2:g.23393636T=	GRCh38
NC_000014.8:g.23862845T= , CM000676.1:g.23862845T=	GRCh37
NC_000014.7:g.22932685T=	NCBI36
NG_023444.1:g.19642A= , LRG_389:g.19642A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405093.9:c.2928+30A= MANE Select	ENSP00000386041.3:n.2928+30A=
ENST00000356287.3:c.2928+30A=	ENSP00000348634.3:n.2928+30A=
ENST00000405093.7:c.2928+30A=	ENSP00000386041.3:n.2928+30A=
NM_002471.3:c.2928+30A= , LRG_389t1:c.2928+30A=	NP_002462.2:n.2928+30A=
NM_002471.4:c.2928+30A= MANE Select	NP_002462.2:n.2928+30A=