Canonical Allele Identifier: CA2123455621

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23424751G= , CM000676.2:g.23424751G=	GRCh38
NC_000014.8:g.23893960G= , CM000676.1:g.23893960G=	GRCh37
NC_000014.7:g.22963800G=	NCBI36
NG_007884.1:g.15911C= , LRG_384:g.15911C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.2679+18C= MANE Select	ENSP00000347507.3:n.2679+18C=
ENST00000355349.3:c.2679+18C=	ENSP00000347507.3:n.2679+18C=
NM_000257.3:c.2679+18C=	NP_000248.2:n.2679+18C=
XR_245686.3:n.2785+18C=
XM_017021340.1:c.2679+18C=	XP_016876829.1:n.2679+18C=
NM_000257.4:c.2679+18C= MANE Select	NP_000248.2:n.2679+18C=