Canonical Allele Identifier: CA2123413477

Gene: MYH6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23392894G= , CM000676.2:g.23392894G=	GRCh38
NC_000014.8:g.23862103G= , CM000676.1:g.23862103G=	GRCh37
NC_000014.7:g.22931943G=	NCBI36
NG_023444.1:g.20384C= , LRG_389:g.20384C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405093.9:c.3251+18C= MANE Select	ENSP00000386041.3:n.3251+18C=
ENST00000356287.3:c.3251+18C=	ENSP00000348634.3:n.3251+18C=
ENST00000405093.7:c.3251+18C=	ENSP00000386041.3:n.3251+18C=
NM_002471.3:c.3251+18C= , LRG_389t1:c.3251+18C=	NP_002462.2:n.3251+18C=
NM_002471.4:c.3251+18C= MANE Select	NP_002462.2:n.3251+18C=