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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:
CA408405378
Gene: THBD
HGNC
NCBI
Linked Data
dbSNP Id:
rs1984620329
MyVariant Identifiers:
chr20:g.23028632T>C (hg19)
chr20:g.23047995T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.23047995T>C , CM000682.2:g.23047995T>C
GRCh38
NC_000020.10:g.23028632T>C , CM000682.1:g.23028632T>C
GRCh37
NC_000020.9:g.22976632T>C
NCBI36
NG_012027.1:g.6670A>G , LRG_168:g.6670A>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000377103.3:c.1510A>G
MANE Select
ENSP00000366307.2:p.Thr504Ala
ENST00000377103.2:c.1510A>G
ENSP00000366307.2:p.Thr504Ala
NM_000361.2:c.1510A>G , LRG_168t1:c.1510A>G
NP_000352.1:p.Thr504Ala
NM_000361.3:c.1510A>G
MANE Select
NP_000352.1:p.Thr504Ala
Search 100 bp 5'
Search 100 bp 3'