Canonical Allele Identifier: CA485609922

Gene: MYH6

Linked Data

• MyVariant Identifiers: chr14:g.23865522G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23396313G>A , CM000676.2:g.23396313G>A	GRCh38
NC_000014.8:g.23865522G>A , CM000676.1:g.23865522G>A	GRCh37
NC_000014.7:g.22935362G>A	NCBI36
NG_023444.1:g.16965C>T , LRG_389:g.16965C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405093.9:c.2400C>T MANE Select	ENSP00000386041.3:p.Arg800=
ENST00000356287.3:c.2400C>T	ENSP00000348634.3:p.Arg800=
ENST00000405093.7:c.2400C>T	ENSP00000386041.3:p.Arg800=
NM_002471.3:c.2400C>T , LRG_389t1:c.2400C>T	NP_002462.2:p.Arg800=
NM_002471.4:c.2400C>T MANE Select	NP_002462.2:p.Arg800=