Canonical Allele Identifier: CA2800875286
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431680_23431762del , CM000676.2:g.23431680_23431762del GRCh38
NC_000014.8:g.23900889_23900971del , CM000676.1:g.23900889_23900971del GRCh37
NC_000014.7:g.22970729_22970811del NCBI36
NG_007884.1:g.8903_8985del , LRG_384:g.8903_8985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.639+2_640del
ENST00000355349.3:c.639+2_640del
NM_000257.3:c.639+2_640del
XR_245686.3:n.745+2_746del
XM_017021340.1:c.639+2_640del
NM_000257.4:c.639+2_640del