Canonical Allele Identifier: CA2562179035

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431557C>A , CM000676.2:g.23431557C>A	GRCh38
NC_000014.8:g.23900766C>A , CM000676.1:g.23900766C>A	GRCh37
NC_000014.7:g.22970606C>A	NCBI36
NG_007884.1:g.9105G>T , LRG_384:g.9105G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.732+28G>T MANE Select	ENSP00000347507.3:n.732+28G>T
ENST00000355349.3:c.732+28G>T	ENSP00000347507.3:n.732+28G>T
NM_000257.3:c.732+28G>T	NP_000248.2:n.732+28G>T
XR_245686.3:n.838+28G>T
XM_017021340.1:c.732+28G>T	XP_016876829.1:n.732+28G>T
NM_000257.4:c.732+28G>T MANE Select	NP_000248.2:n.732+28G>T