Canonical Allele Identifier: CA257825863
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs879741504

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431482_23431584del , CM000676.2:g.23431482_23431584del GRCh38
NC_000014.8:g.23900691_23900793del , CM000676.1:g.23900691_23900793del GRCh37
NC_000014.7:g.22970531_22970633del NCBI36
NG_007884.1:g.9079_9181del , LRG_384:g.9079_9181del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.732+2_733del
ENST00000355349.3:c.732+2_733del
NM_000257.3:c.732+2_733del
XR_245686.3:n.838+2_839del
XM_017021340.1:c.732+2_733del
NM_000257.4:c.732+2_733del