Canonical Allele Identifier: CA620304255
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1278705273
gnomAD v2: 16-223091-A-G
gnomAD v4: 16-173092-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173092A>G , CM000678.2:g.173092A>G GRCh38
NC_000016.9:g.223091A>G , CM000678.1:g.223091A>G GRCh37
NC_000016.8:g.163091A>G NCBI36
NG_000006.1:g.33955A>G
NG_059186.1:g.1442A>G
NG_059271.1:g.5246A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-33A>G MANE Select ENSP00000251595.6:n.96-33A>G
ENST00000251595.10:c.96-33A>G ENSP00000251595.6:n.96-33A>G
ENST00000397806.1:c.-1-33A>G ENSP00000380908.1:n.-1-33A>G
ENST00000482565.1:n.199A>G
ENST00000484216.1:n.65-33A>G
NM_000517.4:c.96-33A>G NP_000508.1:n.96-33A>G
NM_000517.6:c.96-33A>G MANE Select NP_000508.1:n.96-33A>G