Canonical Allele Identifier: CA485627175

Gene: MYH7

Linked Data

• MyVariant Identifiers: chr14:g.23902885T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433676T>A , CM000676.2:g.23433676T>A	GRCh38
NC_000014.8:g.23902885T>A , CM000676.1:g.23902885T>A	GRCh37
NC_000014.7:g.22972725T>A	NCBI36
NG_007884.1:g.6986A>T , LRG_384:g.6986A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.57A>T MANE Select	ENSP00000347507.3:p.Ser19=
ENST00000355349.3:c.57A>T	ENSP00000347507.3:p.Ser19=
NM_000257.3:c.57A>T	NP_000248.2:p.Ser19=
XR_245686.3:n.163A>T
XM_017021340.1:c.57A>T	XP_016876829.1:p.Ser19=
NM_000257.4:c.57A>T MANE Select	NP_000248.2:p.Ser19=