Canonical Allele Identifier: CA016308
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43077
ClinVar RCV Id: RCV000035972 RCV001852733
dbSNP Id: rs397516249
MyVariant Identifiers: chr14:g.23901049T>C (hg19) chr14:g.23431840T>C (hg38)
PubMed: PMID:27247418
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431840T>C , CM000676.2:g.23431840T>C GRCh38
NC_000014.8:g.23901049T>C , CM000676.1:g.23901049T>C GRCh37
NC_000014.7:g.22970889T>C NCBI36
NG_007884.1:g.8822A>G , LRG_384:g.8822A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.560A>G MANE Select ENSP00000347507.3:p.Asn187Ser
ENST00000355349.3:c.560A>G ENSP00000347507.3:p.Asn187Ser
NM_000257.3:c.560A>G NP_000248.2:p.Asn187Ser
XR_245686.3:n.666A>G
XM_017021340.1:c.560A>G XP_016876829.1:p.Asn187Ser
NM_000257.4:c.560A>G MANE Select NP_000248.2:p.Asn187Ser
Search 100 bp 5'
Search 100 bp 3'