×
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
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA016907
Gene: MYH7
HGNC
NCBI
Linked Data
ClinVar Variation Id:
155812
ClinVar RCV Id:
RCV000143920
dbSNP Id:
rs587782961
MyVariant Identifiers:
chr14:g.23900145T>C (hg19)
chr14:g.23430936T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.23430936T>C , CM000676.2:g.23430936T>C
GRCh38
NC_000014.8:g.23900145T>C , CM000676.1:g.23900145T>C
GRCh37
NC_000014.7:g.22969985T>C
NCBI36
NG_007884.1:g.9726A>G , LRG_384:g.9726A>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000355349.4:c.860A>G
MANE Select
ENSP00000347507.3:p.Tyr287Cys
ENST00000355349.3:c.860A>G
ENSP00000347507.3:p.Tyr287Cys
NM_000257.3:c.860A>G
NP_000248.2:p.Tyr287Cys
XR_245686.3:n.966A>G
XM_017021340.1:c.860A>G
XP_016876829.1:p.Tyr287Cys
NM_000257.4:c.860A>G
MANE Select
NP_000248.2:p.Tyr287Cys
Search 100 bp 5'
Search 100 bp 3'