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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:
CA276415497
Gene: HBA2
HGNC
NCBI
Linked Data
dbSNP Id:
rs41514946
MyVariant Identifiers:
chr16:g.223572C>G (hg19)
chr16:g.173573C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.173573C>G , CM000678.2:g.173573C>G
GRCh38
NC_000016.9:g.223572C>G , CM000678.1:g.223572C>G
GRCh37
NC_000016.8:g.163572C>G
NCBI36
NG_000006.1:g.34436C>G
NG_059186.1:g.1923C>G
NG_059271.1:g.5727C>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000251595.11:c.402C>G
MANE Select
ENSP00000251595.6:p.Ser134Arg
ENST00000251595.10:c.402C>G
ENSP00000251595.6:p.Ser134Arg
ENST00000397806.1:c.306C>G
ENSP00000380908.1:p.Ser102Arg
ENST00000482565.1:n.538C>G
NM_000517.4:c.402C>G
NP_000508.1:p.Ser134Arg
NM_000517.6:c.402C>G
MANE Select
NP_000508.1:p.Ser134Arg
Search 100 bp 5'
Search 100 bp 3'