Canonical Allele Identifier: CA2123442674
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23427889C= , CM000676.2:g.23427889C= GRCh38
NC_000014.8:g.23897098C= , CM000676.1:g.23897098C= GRCh37
NC_000014.7:g.22966938C= NCBI36
NG_007884.1:g.12773G= , LRG_384:g.12773G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.1584G= MANE Select ENSP00000347507.3:p.Met528=
ENST00000355349.3:c.1584G= ENSP00000347507.3:p.Met528=
NM_000257.3:c.1584G= NP_000248.2:p.Met528=
XR_245686.3:n.1690G=
XM_017021340.1:c.1584G= XP_016876829.1:p.Met528=
NM_000257.4:c.1584G= MANE Select NP_000248.2:p.Met528=