Canonical Allele Identifier: CA2200880840
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1902055605
gnomAD v3: 16-173411-G-A
gnomAD v4: 16-173411-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173411G>A , CM000678.2:g.173411G>A GRCh38
NC_000016.9:g.223410G>A , CM000678.1:g.223410G>A GRCh37
NC_000016.8:g.163410G>A NCBI36
NG_000006.1:g.34274G>A
NG_059186.1:g.1761G>A
NG_059271.1:g.5565G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-61G>A MANE Select ENSP00000251595.6:n.301-61G>A
ENST00000251595.10:c.301-61G>A ENSP00000251595.6:n.301-61G>A
ENST00000397806.1:c.205-61G>A ENSP00000380908.1:n.205-61G>A
ENST00000482565.1:n.437-61G>A
ENST00000484216.1:n.351G>A
NM_000517.4:c.301-61G>A NP_000508.1:n.301-61G>A
NM_000517.6:c.301-61G>A MANE Select NP_000508.1:n.301-61G>A
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