Canonical Allele Identifier: CA2630737149
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173086-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173086G>A , CM000678.2:g.173086G>A GRCh38
NC_000016.9:g.223085G>A , CM000678.1:g.223085G>A GRCh37
NC_000016.8:g.163085G>A NCBI36
NG_000006.1:g.33949G>A
NG_059186.1:g.1436G>A
NG_059271.1:g.5240G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-39G>A MANE Select ENSP00000251595.6:n.96-39G>A
ENST00000251595.10:c.96-39G>A ENSP00000251595.6:n.96-39G>A
ENST00000397806.1:c.-1-39G>A ENSP00000380908.1:n.-1-39G>A
ENST00000482565.1:n.193G>A
ENST00000484216.1:n.65-39G>A
NM_000517.4:c.96-39G>A NP_000508.1:n.96-39G>A
NM_000517.6:c.96-39G>A MANE Select NP_000508.1:n.96-39G>A
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