Canonical Allele Identifier: CA2123458087

Gene: MYH7

Linked Data

• dbSNP Id: rs1892665497

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425674T>A , CM000676.2:g.23425674T>A	GRCh38
NC_000014.8:g.23894883T>A , CM000676.1:g.23894883T>A	GRCh37
NC_000014.7:g.22964723T>A	NCBI36
NG_007884.1:g.14988A>T , LRG_384:g.14988A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2286+21A>T MANE Select	ENSP00000347507.3:n.2286+21A>T
ENST00000355349.3:c.2286+21A>T	ENSP00000347507.3:n.2286+21A>T
NM_000257.3:c.2286+21A>T	NP_000248.2:n.2286+21A>T
XR_245686.3:n.2392+21A>T
XM_017021340.1:c.2286+21A>T	XP_016876829.1:n.2286+21A>T
NM_000257.4:c.2286+21A>T MANE Select	NP_000248.2:n.2286+21A>T