Canonical Allele Identifier: CA2123456396
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433909C= , CM000676.2:g.23433909C= GRCh38
NC_000014.8:g.23903118C= , CM000676.1:g.23903118C= GRCh37
NC_000014.7:g.22972958C= NCBI36
NG_007884.1:g.6753G= , LRG_384:g.6753G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-8-169G= MANE Select ENSP00000347507.3:n.-8-169G=
ENST00000355349.3:c.-8-169G= ENSP00000347507.3:n.-8-169G=
NM_000257.3:c.-8-169G= NP_000248.2:n.-8-169G=
XR_245686.3:n.99-169G=
XM_017021340.1:c.-8-169G= XP_016876829.1:n.-8-169G=
NM_000257.4:c.-8-169G= MANE Select NP_000248.2:n.-8-169G=