Canonical Allele Identifier: CA257825866
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1555338647

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431482_23431585delinsA , CM000676.2:g.23431482_23431585delinsA GRCh38
NC_000014.8:g.23900691_23900794delinsA , CM000676.1:g.23900691_23900794delinsA GRCh37
NC_000014.7:g.22970531_22970634delinsA NCBI36
NG_007884.1:g.9077_9180delinsT , LRG_384:g.9077_9180delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.732_733-1delinsT
ENST00000355349.3:c.732_733-1delinsT
NM_000257.3:c.732_733-1delinsT
XR_245686.3:n.838_839-1delinsT
XM_017021340.1:c.732_733-1delinsT
NM_000257.4:c.732_733-1delinsT