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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:
CA389035226
Gene: MYH7
HGNC
NCBI
Linked Data
ClinVar Variation Id:
659010
ClinVar RCV Id:
RCV000815943
dbSNP Id:
rs1353101205
MyVariant Identifiers:
chr14:g.23884288C>A (hg19)
chr14:g.23415079C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.23415079C>A , CM000676.2:g.23415079C>A
GRCh38
NC_000014.8:g.23884288C>A , CM000676.1:g.23884288C>A
GRCh37
NC_000014.7:g.22954128C>A
NCBI36
NG_007884.1:g.25583G>T , LRG_384:g.25583G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000355349.4:c.5475G>T
MANE Select
ENSP00000347507.3:p.Glu1825Asp
ENST00000355349.3:c.5475G>T
ENSP00000347507.3:p.Glu1825Asp
NM_000257.3:c.5475G>T
NP_000248.2:p.Glu1825Asp
XM_017021340.1:c.5475G>T
XP_016876829.1:p.Glu1825Asp
NM_000257.4:c.5475G>T
MANE Select
NP_000248.2:p.Glu1825Asp
Search 100 bp 5'
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