Canonical Allele Identifier: CA2123414013

Gene: MYH6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23393608A= , CM000676.2:g.23393608A=	GRCh38
NC_000014.8:g.23862817A= , CM000676.1:g.23862817A=	GRCh37
NC_000014.7:g.22932657A=	NCBI36
NG_023444.1:g.19670T= , LRG_389:g.19670T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405093.9:c.2928+58T= MANE Select	ENSP00000386041.3:n.2928+58T=
ENST00000356287.3:c.2928+58T=	ENSP00000348634.3:n.2928+58T=
ENST00000405093.7:c.2928+58T=	ENSP00000386041.3:n.2928+58T=
NM_002471.3:c.2928+58T= , LRG_389t1:c.2928+58T=	NP_002462.2:n.2928+58T=
NM_002471.4:c.2928+58T= MANE Select	NP_002462.2:n.2928+58T=