Canonical Allele Identifier: CA013459
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164305
ClinVar RCV Id: RCV000151251 RCV000766443
dbSNP Id: rs192722540
MyVariant Identifiers: chr14:g.23891399G>C (hg19) chr14:g.23422190G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422190G>C , CM000676.2:g.23422190G>C GRCh38
NC_000014.8:g.23891399G>C , CM000676.1:g.23891399G>C GRCh37
NC_000014.7:g.22961239G>C NCBI36
NG_007884.1:g.18472C>G , LRG_384:g.18472C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.3235C>G MANE Select ENSP00000347507.3:p.Arg1079Gly
ENST00000355349.3:c.3235C>G ENSP00000347507.3:p.Arg1079Gly
NM_000257.3:c.3235C>G NP_000248.2:p.Arg1079Gly
XR_245686.3:n.3341C>G
XM_017021340.1:c.3235C>G XP_016876829.1:p.Arg1079Gly
NM_000257.4:c.3235C>G MANE Select NP_000248.2:p.Arg1079Gly
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