Canonical Allele Identifier: CA2123450242
Gene: MYH7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23430889G= , CM000676.2:g.23430889G= GRCh38
NC_000014.8:g.23900098G= , CM000676.1:g.23900098G= GRCh37
NC_000014.7:g.22969938G= NCBI36
NG_007884.1:g.9773C= , LRG_384:g.9773C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.895+12C= MANE Select ENSP00000347507.3:n.895+12C=
ENST00000355349.3:c.895+12C= ENSP00000347507.3:n.895+12C=
NM_000257.3:c.895+12C= NP_000248.2:n.895+12C=
XR_245686.3:n.1001+12C=
XM_017021340.1:c.895+12C= XP_016876829.1:n.895+12C=
NM_000257.4:c.895+12C= MANE Select NP_000248.2:n.895+12C=
Search 100 bp 5'
Search 100 bp 3'