Canonical Allele Identifier: CA2200880590
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173081G= , CM000678.2:g.173081G= GRCh38
NC_000016.9:g.223080G= , CM000678.1:g.223080G= GRCh37
NC_000016.8:g.163080G= NCBI36
NG_000006.1:g.33944G=
NG_059186.1:g.1431G=
NG_059271.1:g.5235G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-44G= MANE Select ENSP00000251595.6:n.96-44G=
ENST00000251595.10:c.96-44G= ENSP00000251595.6:n.96-44G=
ENST00000397806.1:c.-1-44G= ENSP00000380908.1:n.-1-44G=
ENST00000482565.1:n.188G=
ENST00000484216.1:n.65-44G=
NM_000517.4:c.96-44G= NP_000508.1:n.96-44G=
NM_000517.6:c.96-44G= MANE Select NP_000508.1:n.96-44G=