Canonical Allele Identifier: CA2630737142
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173076-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173076T>G , CM000678.2:g.173076T>G GRCh38
NC_000016.9:g.223075T>G , CM000678.1:g.223075T>G GRCh37
NC_000016.8:g.163075T>G NCBI36
NG_000006.1:g.33939T>G
NG_059186.1:g.1426T>G
NG_059271.1:g.5230T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.96-49T>G MANE Select ENSP00000251595.6:n.96-49T>G
ENST00000251595.10:c.96-49T>G ENSP00000251595.6:n.96-49T>G
ENST00000397806.1:c.-1-49T>G ENSP00000380908.1:n.-1-49T>G
ENST00000482565.1:n.183T>G
ENST00000484216.1:n.65-49T>G
NM_000517.4:c.96-49T>G NP_000508.1:n.96-49T>G
NM_000517.6:c.96-49T>G MANE Select NP_000508.1:n.96-49T>G
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