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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:
CA125885
Gene: HBA1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
15813
ClinVar RCV Id:
RCV000017154
RCV000017155
dbSNP Id:
rs36024711
MyVariant Identifiers:
chr16:g.226996A>G (hg19)
chr16:g.176997A>G (hg38)
PubMed:
PMID:14236737
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.176997A>G , CM000678.2:g.176997A>G
GRCh38
NC_000016.9:g.226996A>G , CM000678.1:g.226996A>G
GRCh37
NC_000016.8:g.166996A>G
NCBI36
NG_000006.1:g.37860A>G
NG_059186.1:g.5347A>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000320868.9:c.164A>G
MANE Select
ENSP00000322421.5:p.Gln55Arg
ENST00000397797.1:c.68A>G
ENSP00000380899.1:p.Gln23Arg
ENST00000472694.1:n.300A>G
ENST00000487791.1:n.133A>G
NM_000558.4:c.164A>G
NP_000549.1:p.Gln55Arg
NM_000558.5:c.164A>G
MANE Select
NP_000549.1:p.Gln55Arg
Search 100 bp 5'
Search 100 bp 3'