Canonical Allele Identifier: CA2838227691

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420936C>A , CM000676.2:g.23420936C>A	GRCh38
NC_000014.8:g.23890145C>A , CM000676.1:g.23890145C>A	GRCh37
NC_000014.7:g.22959985C>A	NCBI36
NG_007884.1:g.19726G>T , LRG_384:g.19726G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3336+22G>T MANE Select	ENSP00000347507.3:n.3336+22G>T
ENST00000355349.3:c.3336+22G>T	ENSP00000347507.3:n.3336+22G>T
NM_000257.3:c.3336+22G>T	NP_000248.2:n.3336+22G>T
XR_245686.3:n.3444+22G>T
XM_017021340.1:c.3336+22G>T	XP_016876829.1:n.3336+22G>T
NM_000257.4:c.3336+22G>T MANE Select	NP_000248.2:n.3336+22G>T