Canonical Allele Identifier: CA2123452366
Gene: MYH7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431694G= , CM000676.2:g.23431694G= GRCh38
NC_000014.8:g.23900903G= , CM000676.1:g.23900903G= GRCh37
NC_000014.7:g.22970743G= NCBI36
NG_007884.1:g.8968C= , LRG_384:g.8968C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.640-17C= MANE Select ENSP00000347507.3:n.640-17C=
ENST00000355349.3:c.640-17C= ENSP00000347507.3:n.640-17C=
NM_000257.3:c.640-17C= NP_000248.2:n.640-17C=
XR_245686.3:n.746-17C=
XM_017021340.1:c.640-17C= XP_016876829.1:n.640-17C=
NM_000257.4:c.640-17C= MANE Select NP_000248.2:n.640-17C=
Search 100 bp 5'
Search 100 bp 3'