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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:
CA048280
Gene: MYH7
HGNC
NCBI
Linked Data
ClinVar Variation Id:
379296
ClinVar RCV Id:
RCV000426845
RCV002061605
dbSNP Id:
rs199975761
ExAC:
14:23882953 A / C
gnomAD v2:
14-23882953-A-C
gnomAD v3:
14-23413744-A-C
gnomAD v4:
14-23413744-A-C
MyVariant Identifiers:
chr14:g.23882953A>C (hg19)
chr14:g.23413744A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.23413744A>C , CM000676.2:g.23413744A>C
GRCh38
NC_000014.8:g.23882953A>C , CM000676.1:g.23882953A>C
GRCh37
NC_000014.7:g.22952793A>C
NCBI36
NG_007884.1:g.26918T>G , LRG_384:g.26918T>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000355349.4:c.5790+15T>G
MANE Select
ENSP00000347507.3:n.5790+15T>G
ENST00000355349.3:c.5790+15T>G
ENSP00000347507.3:n.5790+15T>G
NM_000257.3:c.5790+15T>G
NP_000248.2:n.5790+15T>G
XM_017021340.1:c.5790+15T>G
XP_016876829.1:n.5790+15T>G
NM_000257.4:c.5790+15T>G
MANE Select
NP_000248.2:n.5790+15T>G
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