Canonical Allele Identifier: CA492994634
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1327047505
MyVariant Identifiers: chr16:g.223220C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173221C>G , CM000678.2:g.173221C>G GRCh38
NC_000016.9:g.223220C>G , CM000678.1:g.223220C>G GRCh37
NC_000016.8:g.163220C>G NCBI36
NG_000006.1:g.34084C>G
NG_059186.1:g.1571C>G
NG_059271.1:g.5375C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.192C>G MANE Select ENSP00000251595.6:p.Ala64=
ENST00000251595.10:c.192C>G ENSP00000251595.6:p.Ala64=
ENST00000397806.1:c.96C>G ENSP00000380908.1:p.Ala32=
ENST00000482565.1:n.328C>G
ENST00000484216.1:n.161C>G
NM_000517.4:c.192C>G NP_000508.1:p.Ala64=
NM_000517.6:c.192C>G MANE Select NP_000508.1:p.Ala64=
Search 100 bp 5'
Search 100 bp 3'