Canonical Allele Identifier: CA2575852755
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173073C>A , CM000678.2:g.173073C>A GRCh38
NC_000016.9:g.223072C>A , CM000678.1:g.223072C>A GRCh37
NC_000016.8:g.163072C>A NCBI36
NG_000006.1:g.33936C>A
NG_059186.1:g.1423C>A
NG_059271.1:g.5227C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.96-52C>A MANE Select ENSP00000251595.6:n.96-52C>A
ENST00000251595.10:c.96-52C>A ENSP00000251595.6:n.96-52C>A
ENST00000397806.1:c.-1-52C>A ENSP00000380908.1:n.-1-52C>A
ENST00000482565.1:n.180C>A
ENST00000484216.1:n.65-52C>A
NM_000517.4:c.96-52C>A NP_000508.1:n.96-52C>A
NM_000517.6:c.96-52C>A MANE Select NP_000508.1:n.96-52C>A