Canonical Allele Identifier: CA485610003

Gene: MYH6

Linked Data

• MyVariant Identifiers: chr14:g.23865578T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23396369T>G , CM000676.2:g.23396369T>G	GRCh38
NC_000014.8:g.23865578T>G , CM000676.1:g.23865578T>G	GRCh37
NC_000014.7:g.22935418T>G	NCBI36
NG_023444.1:g.16909A>C , LRG_389:g.16909A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405093.9:c.2344A>C MANE Select	ENSP00000386041.3:p.Arg782=
ENST00000356287.3:c.2344A>C	ENSP00000348634.3:p.Arg782=
ENST00000405093.7:c.2344A>C	ENSP00000386041.3:p.Arg782=
NM_002471.3:c.2344A>C , LRG_389t1:c.2344A>C	NP_002462.2:p.Arg782=
NM_002471.4:c.2344A>C MANE Select	NP_002462.2:p.Arg782=