Canonical Allele Identifier: CA2123452980
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423547A= , CM000676.2:g.23423547A= GRCh38
NC_000014.8:g.23892756A= , CM000676.1:g.23892756A= GRCh37
NC_000014.7:g.22962596A= NCBI36
NG_007884.1:g.17115T= , LRG_384:g.17115T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099T= MANE Select ENSP00000347507.3:p.Asp1033=
ENST00000355349.3:c.3099T= ENSP00000347507.3:p.Asp1033=
NM_000257.3:c.3099T= NP_000248.2:p.Asp1033=
XR_245686.3:n.3205T=
XM_017021340.1:c.3099T= XP_016876829.1:p.Asp1033=
NM_000257.4:c.3099T= MANE Select NP_000248.2:p.Asp1033=