Canonical Allele Identifier: CA389037913
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2805702
ClinVar RCV Id: RCV003749374
MyVariant Identifiers: chr14:g.23885507G>C (hg19) chr14:g.23416298G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416298G>C , CM000676.2:g.23416298G>C GRCh38
NC_000014.8:g.23885507G>C , CM000676.1:g.23885507G>C GRCh37
NC_000014.7:g.22955347G>C NCBI36
NG_007884.1:g.24364C>G , LRG_384:g.24364C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4659C>G (MYH7) MANE Select ENSP00000347507.3:p.His1553Gln
ENST00000355349.3:c.4659C>G (MYH7) ENSP00000347507.3:p.His1553Gln
NM_000257.3:c.4659C>G (MYH7) NP_000248.2:p.His1553Gln
NR_126491.1:n.558+1G>C (MHRT)
XM_017021340.1:c.4659C>G (MYH7) XP_016876829.1:p.His1553Gln
NM_000257.4:c.4659C>G (MYH7) MANE Select NP_000248.2:p.His1553Gln
Search 100 bp 5'
Search 100 bp 3'