Canonical Allele Identifier: CA279325
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 217474
ClinVar RCV Id: RCV000201507 RCV003586167
dbSNP Id: rs863225103
MyVariant Identifiers: chr14:g.23894133T>C (hg19) chr14:g.23424924T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424924T>C , CM000676.2:g.23424924T>C GRCh38
NC_000014.8:g.23894133T>C , CM000676.1:g.23894133T>C GRCh37
NC_000014.7:g.22963973T>C NCBI36
NG_007884.1:g.15738A>G , LRG_384:g.15738A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2524A>G MANE Select ENSP00000347507.3:p.Ser842Gly
ENST00000355349.3:c.2524A>G ENSP00000347507.3:p.Ser842Gly
NM_000257.3:c.2524A>G NP_000248.2:p.Ser842Gly
XR_245686.3:n.2630A>G
XM_017021340.1:c.2524A>G XP_016876829.1:p.Ser842Gly
NM_000257.4:c.2524A>G MANE Select NP_000248.2:p.Ser842Gly
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