×
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:
CA125709
Gene: HBA1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
15717
ClinVar RCV Id:
RCV000017011
dbSNP Id:
rs34259907
MyVariant Identifiers:
chr16:g.227013A>G (hg19)
chr16:g.177014A>G (hg38)
PubMed:
PMID:3108202
PMID:6783600
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.177014A>G , CM000678.2:g.177014A>G
GRCh38
NC_000016.9:g.227013A>G , CM000678.1:g.227013A>G
GRCh37
NC_000016.8:g.167013A>G
NCBI36
NG_000006.1:g.37877A>G
NG_059186.1:g.5364A>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000320868.9:c.181A>G
MANE Select
ENSP00000322421.5:p.Lys61Glu
ENST00000397797.1:c.85A>G
ENSP00000380899.1:p.Lys29Glu
ENST00000472694.1:n.317A>G
ENST00000487791.1:n.150A>G
NM_000558.4:c.181A>G
NP_000549.1:p.Lys61Glu
NM_000558.5:c.181A>G
MANE Select
NP_000549.1:p.Lys61Glu
Search 100 bp 5'
Search 100 bp 3'