Canonical Allele Identifier: CA2123457843
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413756C= , CM000676.2:g.23413756C= GRCh38
NC_000014.8:g.23882965C= , CM000676.1:g.23882965C= GRCh37
NC_000014.7:g.22952805C= NCBI36
NG_007884.1:g.26906G= , LRG_384:g.26906G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5790+3G= MANE Select ENSP00000347507.3:n.5790+3G=
ENST00000355349.3:c.5790+3G= ENSP00000347507.3:n.5790+3G=
NM_000257.3:c.5790+3G= NP_000248.2:n.5790+3G=
XM_017021340.1:c.5790+3G= XP_016876829.1:n.5790+3G=
NM_000257.4:c.5790+3G= MANE Select NP_000248.2:n.5790+3G=