Canonical Allele Identifier: CA2200880304
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172959G= , CM000678.2:g.172959G= GRCh38
NC_000016.9:g.222958G= , CM000678.1:g.222958G= GRCh37
NC_000016.8:g.162958G= NCBI36
NG_000006.1:g.33822G=
NG_059186.1:g.1309G=
NG_059271.1:g.5113G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.47G= MANE Select ENSP00000251595.6:p.Gly16=
ENST00000251595.10:c.47G= ENSP00000251595.6:p.Gly16=
ENST00000397806.1:c.-2+1G= ENSP00000380908.1:n.-2+1G=
ENST00000482565.1:n.66G=
ENST00000484216.1:n.16G=
NM_000517.4:c.47G= NP_000508.1:p.Gly16=
NM_000517.6:c.47G= MANE Select NP_000508.1:p.Gly16=