Canonical Allele Identifier: CA012431
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs730880897

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424974T>C , CM000676.2:g.23424974T>C GRCh38
NC_000014.8:g.23894183T>C , CM000676.1:g.23894183T>C GRCh37
NC_000014.7:g.22964023T>C NCBI36
NG_007884.1:g.15688A>G , LRG_384:g.15688A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2474A>G MANE Select ENSP00000347507.3:p.Lys825Arg
ENST00000355349.3:c.2474A>G ENSP00000347507.3:p.Lys825Arg
NM_000257.3:c.2474A>G NP_000248.2:p.Lys825Arg
XR_245686.3:n.2580A>G
XM_017021340.1:c.2474A>G XP_016876829.1:p.Lys825Arg
NM_000257.4:c.2474A>G MANE Select NP_000248.2:p.Lys825Arg