Canonical Allele Identifier: CA613317723
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 518180
dbSNP Id: rs1227114881

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423904T>C , CM000676.2:g.23423904T>C GRCh38
NC_000014.8:g.23893113T>C , CM000676.1:g.23893113T>C GRCh37
NC_000014.7:g.22962953T>C NCBI36
NG_007884.1:g.16758A>G , LRG_384:g.16758A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2922+3A>G MANE Select ENSP00000347507.3:n.2922+3A>G
ENST00000355349.3:c.2922+3A>G ENSP00000347507.3:n.2922+3A>G
NM_000257.3:c.2922+3A>G NP_000248.2:n.2922+3A>G
XR_245686.3:n.3028+3A>G
XM_017021340.1:c.2922+3A>G XP_016876829.1:n.2922+3A>G
NM_000257.4:c.2922+3A>G MANE Select NP_000248.2:n.2922+3A>G