Canonical Allele Identifier: CA389051985
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 518590
dbSNP Id: rs1555338578

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23430981C>G , CM000676.2:g.23430981C>G GRCh38
NC_000014.8:g.23900190C>G , CM000676.1:g.23900190C>G GRCh37
NC_000014.7:g.22970030C>G NCBI36
NG_007884.1:g.9681G>C , LRG_384:g.9681G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.815G>C MANE Select ENSP00000347507.3:p.Arg272Thr
ENST00000355349.3:c.815G>C ENSP00000347507.3:p.Arg272Thr
NM_000257.3:c.815G>C NP_000248.2:p.Arg272Thr
XR_245686.3:n.921G>C
XM_017021340.1:c.815G>C XP_016876829.1:p.Arg272Thr
NM_000257.4:c.815G>C MANE Select NP_000248.2:p.Arg272Thr