Canonical Allele Identifier: CA2200880612
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173099A= , CM000678.2:g.173099A= GRCh38
NC_000016.9:g.223098A= , CM000678.1:g.223098A= GRCh37
NC_000016.8:g.163098A= NCBI36
NG_000006.1:g.33962A=
NG_059186.1:g.1449A=
NG_059271.1:g.5253A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-26A= MANE Select ENSP00000251595.6:n.96-26A=
ENST00000251595.10:c.96-26A= ENSP00000251595.6:n.96-26A=
ENST00000397806.1:c.-1-26A= ENSP00000380908.1:n.-1-26A=
ENST00000482565.1:n.206A=
ENST00000484216.1:n.65-26A=
NM_000517.4:c.96-26A= NP_000508.1:n.96-26A=
NM_000517.6:c.96-26A= MANE Select NP_000508.1:n.96-26A=