Canonical Allele Identifier: CA2123453643
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423772G= , CM000676.2:g.23423772G= GRCh38
NC_000014.8:g.23892981G= , CM000676.1:g.23892981G= GRCh37
NC_000014.7:g.22962821G= NCBI36
NG_007884.1:g.16890C= , LRG_384:g.16890C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2923-49C= MANE Select ENSP00000347507.3:n.2923-49C=
ENST00000355349.3:c.2923-49C= ENSP00000347507.3:n.2923-49C=
NM_000257.3:c.2923-49C= NP_000248.2:n.2923-49C=
XR_245686.3:n.3029-49C=
XM_017021340.1:c.2923-49C= XP_016876829.1:n.2923-49C=
NM_000257.4:c.2923-49C= MANE Select NP_000248.2:n.2923-49C=