Canonical Allele Identifier: CA2123456589

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23434080A= , CM000676.2:g.23434080A=	GRCh38
NC_000014.8:g.23903289A= , CM000676.1:g.23903289A=	GRCh37
NC_000014.7:g.22973129A=	NCBI36
NG_007884.1:g.6582T= , LRG_384:g.6582T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.-9+114T= MANE Select	ENSP00000347507.3:n.-9+114T=
ENST00000355349.3:c.-9+114T=	ENSP00000347507.3:n.-9+114T=
NM_000257.3:c.-9+114T=	NP_000248.2:n.-9+114T=
XR_245686.3:n.98+114T=
XM_017021340.1:c.-8-340T=	XP_016876829.1:n.-8-340T=
NM_000257.4:c.-9+114T= MANE Select	NP_000248.2:n.-9+114T=