Canonical Allele Identifier: CA2200880839
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173411G= , CM000678.2:g.173411G= GRCh38
NC_000016.9:g.223410G= , CM000678.1:g.223410G= GRCh37
NC_000016.8:g.163410G= NCBI36
NG_000006.1:g.34274G=
NG_059186.1:g.1761G=
NG_059271.1:g.5565G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-61G= MANE Select ENSP00000251595.6:n.301-61G=
ENST00000251595.10:c.301-61G= ENSP00000251595.6:n.301-61G=
ENST00000397806.1:c.205-61G= ENSP00000380908.1:n.205-61G=
ENST00000482565.1:n.437-61G=
ENST00000484216.1:n.351G=
NM_000517.4:c.301-61G= NP_000508.1:n.301-61G=
NM_000517.6:c.301-61G= MANE Select NP_000508.1:n.301-61G=