Canonical Allele Identifier: CA485616068
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23882983A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413774A>T , CM000676.2:g.23413774A>T GRCh38
NC_000014.8:g.23882983A>T , CM000676.1:g.23882983A>T GRCh37
NC_000014.7:g.22952823A>T NCBI36
NG_007884.1:g.26888T>A , LRG_384:g.26888T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5775T>A MANE Select ENSP00000347507.3:p.Arg1925=
ENST00000355349.3:c.5775T>A ENSP00000347507.3:p.Arg1925=
NM_000257.3:c.5775T>A NP_000248.2:p.Arg1925=
XM_017021340.1:c.5775T>A XP_016876829.1:p.Arg1925=
NM_000257.4:c.5775T>A MANE Select NP_000248.2:p.Arg1925=
Search 100 bp 5'
Search 100 bp 3'