Canonical Allele Identifier: CA2200880846
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1596570209

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173416T>G , CM000678.2:g.173416T>G GRCh38
NC_000016.9:g.223415T>G , CM000678.1:g.223415T>G GRCh37
NC_000016.8:g.163415T>G NCBI36
NG_000006.1:g.34279T>G
NG_059186.1:g.1766T>G
NG_059271.1:g.5570T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-56T>G MANE Select ENSP00000251595.6:n.301-56T>G
ENST00000251595.10:c.301-56T>G ENSP00000251595.6:n.301-56T>G
ENST00000397806.1:c.205-56T>G ENSP00000380908.1:n.205-56T>G
ENST00000482565.1:n.437-56T>G
ENST00000484216.1:n.356T>G
NM_000517.4:c.301-56T>G NP_000508.1:n.301-56T>G
NM_000517.6:c.301-56T>G MANE Select NP_000508.1:n.301-56T>G