Canonical Allele Identifier: CA2200880558
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173046C= , CM000678.2:g.173046C= GRCh38
NC_000016.9:g.223045C= , CM000678.1:g.223045C= GRCh37
NC_000016.8:g.163045C= NCBI36
NG_000006.1:g.33909C=
NG_059186.1:g.1396C=
NG_059271.1:g.5200C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.95+39C= MANE Select ENSP00000251595.6:n.95+39C=
ENST00000251595.10:c.95+39C= ENSP00000251595.6:n.95+39C=
ENST00000397806.1:c.-1-79C= ENSP00000380908.1:n.-1-79C=
ENST00000482565.1:n.153C=
ENST00000484216.1:n.64+39C=
NM_000517.4:c.95+39C= NP_000508.1:n.95+39C=
NM_000517.6:c.95+39C= MANE Select NP_000508.1:n.95+39C=
Search 100 bp 5'
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