Canonical Allele Identifier: CA176969

Gene: MYH6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23405727G>A , CM000676.2:g.23405727G>A	GRCh38
NC_000014.8:g.23874936G>A , CM000676.1:g.23874936G>A	GRCh37
NC_000014.7:g.22944776G>A	NCBI36
NG_023444.1:g.7551C>T , LRG_389:g.7551C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002471.4:c.245C>T MANE Select	NP_002462.2:p.Pro82Leu
ENST00000405093.9:c.245C>T MANE Select	ENSP00000386041.3:p.Pro82Leu
NM_002471.3:c.245C>T , LRG_389t1:c.245C>T	NP_002462.2:p.Pro82Leu
ENST00000356287.3:c.245C>T	ENSP00000348634.3:p.Pro82Leu
ENST00000405093.7:c.245C>T	ENSP00000386041.3:p.Pro82Leu
ENST00000557461.1:n.299C>T
ENST00000557461.2:n.312C>T