Canonical Allele Identifier: CA2200880831
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173402C= , CM000678.2:g.173402C= GRCh38
NC_000016.9:g.223401C= , CM000678.1:g.223401C= GRCh37
NC_000016.8:g.163401C= NCBI36
NG_000006.1:g.34265C=
NG_059186.1:g.1752C=
NG_059271.1:g.5556C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.301-70C= MANE Select ENSP00000251595.6:n.301-70C=
ENST00000251595.10:c.301-70C= ENSP00000251595.6:n.301-70C=
ENST00000397806.1:c.205-70C= ENSP00000380908.1:n.205-70C=
ENST00000482565.1:n.437-70C=
ENST00000484216.1:n.342C=
NM_000517.4:c.301-70C= NP_000508.1:n.301-70C=
NM_000517.6:c.301-70C= MANE Select NP_000508.1:n.301-70C=
Search 100 bp 5'
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