Canonical Allele Identifier: CA2630736725
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-172850-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172850A>G , CM000678.2:g.172850A>G GRCh38
NC_000016.9:g.222849A>G , CM000678.1:g.222849A>G GRCh37
NC_000016.8:g.162849A>G NCBI36
NG_000006.1:g.33713A>G
NG_059186.1:g.1200A>G
NG_059271.1:g.5004A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.10:c.-63A>G ENSP00000251595.6:n.-63A>G
NM_000517.4:c.-63A>G NP_000508.1:n.-63A>G