Canonical Allele Identifier: CA2123456198
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433757C= , CM000676.2:g.23433757C= GRCh38
NC_000014.8:g.23902966C= , CM000676.1:g.23902966C= GRCh37
NC_000014.7:g.22972806C= NCBI36
NG_007884.1:g.6905G= , LRG_384:g.6905G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-8-17G= MANE Select ENSP00000347507.3:n.-8-17G=
ENST00000355349.3:c.-8-17G= ENSP00000347507.3:n.-8-17G=
NM_000257.3:c.-8-17G= NP_000248.2:n.-8-17G=
XR_245686.3:n.99-17G=
XM_017021340.1:c.-8-17G= XP_016876829.1:n.-8-17G=
NM_000257.4:c.-8-17G= MANE Select NP_000248.2:n.-8-17G=