Canonical Allele Identifier: CA2123450730

Gene: MYH7

Linked Data

• dbSNP Id: rs563344535

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431030A>G , CM000676.2:g.23431030A>G	GRCh38
NC_000014.8:g.23900239A>G , CM000676.1:g.23900239A>G	GRCh37
NC_000014.7:g.22970079A>G	NCBI36
NG_007884.1:g.9632T>C , LRG_384:g.9632T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-31T>C MANE Select	ENSP00000347507.3:n.797-31T>C
ENST00000355349.3:c.797-31T>C	ENSP00000347507.3:n.797-31T>C
NM_000257.3:c.797-31T>C	NP_000248.2:n.797-31T>C
XR_245686.3:n.903-31T>C
XM_017021340.1:c.797-31T>C	XP_016876829.1:n.797-31T>C
NM_000257.4:c.797-31T>C MANE Select	NP_000248.2:n.797-31T>C