Canonical Allele Identifier: CA2123456283
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433854G= , CM000676.2:g.23433854G= GRCh38
NC_000014.8:g.23903063G= , CM000676.1:g.23903063G= GRCh37
NC_000014.7:g.22972903G= NCBI36
NG_007884.1:g.6808C= , LRG_384:g.6808C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-8-114C= MANE Select ENSP00000347507.3:n.-8-114C=
ENST00000355349.3:c.-8-114C= ENSP00000347507.3:n.-8-114C=
NM_000257.3:c.-8-114C= NP_000248.2:n.-8-114C=
XR_245686.3:n.99-114C=
XM_017021340.1:c.-8-114C= XP_016876829.1:n.-8-114C=
NM_000257.4:c.-8-114C= MANE Select NP_000248.2:n.-8-114C=