Canonical Allele Identifier: CA2123457721
Gene: MYH7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413713A= , CM000676.2:g.23413713A= GRCh38
NC_000014.8:g.23882922A= , CM000676.1:g.23882922A= GRCh37
NC_000014.7:g.22952762A= NCBI36
NG_007884.1:g.26949T= , LRG_384:g.26949T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5790+46T= MANE Select ENSP00000347507.3:n.5790+46T=
ENST00000355349.3:c.5790+46T= ENSP00000347507.3:n.5790+46T=
NM_000257.3:c.5790+46T= NP_000248.2:n.5790+46T=
XM_017021340.1:c.5790+46T= XP_016876829.1:n.5790+46T=
NM_000257.4:c.5790+46T= MANE Select NP_000248.2:n.5790+46T=
Search 100 bp 5'
Search 100 bp 3'