Canonical Allele Identifier: CA389048139
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 518874
ClinVar RCV Id: RCV000620889
dbSNP Id: rs1555337717
MyVariant Identifiers: chr14:g.23894091A>G (hg19) chr14:g.23424882A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424882A>G , CM000676.2:g.23424882A>G GRCh38
NC_000014.8:g.23894091A>G , CM000676.1:g.23894091A>G GRCh37
NC_000014.7:g.22963931A>G NCBI36
NG_007884.1:g.15780T>C , LRG_384:g.15780T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2566T>C MANE Select ENSP00000347507.3:p.Phe856Leu
ENST00000355349.3:c.2566T>C ENSP00000347507.3:p.Phe856Leu
NM_000257.3:c.2566T>C NP_000248.2:p.Phe856Leu
XR_245686.3:n.2672T>C
XM_017021340.1:c.2566T>C XP_016876829.1:p.Phe856Leu
NM_000257.4:c.2566T>C MANE Select NP_000248.2:p.Phe856Leu
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