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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA016828
Gene: MYH7
HGNC
NCBI
Linked Data
ClinVar Variation Id:
181326
ClinVar RCV Id:
RCV000208372
RCV000223688
dbSNP Id:
rs730880855
MyVariant Identifiers:
chr14:g.23900634T>C (hg19)
chr14:g.23431425T>C (hg38)
PubMed:
PMID:15358028
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.23431425T>C , CM000676.2:g.23431425T>C
GRCh38
NC_000014.8:g.23900634T>C , CM000676.1:g.23900634T>C
GRCh37
NC_000014.7:g.22970474T>C
NCBI36
NG_007884.1:g.9237A>G , LRG_384:g.9237A>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000355349.4:c.789A>G
MANE Select
ENSP00000347507.3:p.Ile263Met
ENST00000355349.3:c.789A>G
ENSP00000347507.3:p.Ile263Met
NM_000257.3:c.789A>G
NP_000248.2:p.Ile263Met
XR_245686.3:n.895A>G
XM_017021340.1:c.789A>G
XP_016876829.1:p.Ile263Met
NM_000257.4:c.789A>G
MANE Select
NP_000248.2:p.Ile263Met
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