Canonical Allele Identifier: CA2200880579
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173062G= , CM000678.2:g.173062G= GRCh38
NC_000016.9:g.223061G= , CM000678.1:g.223061G= GRCh37
NC_000016.8:g.163061G= NCBI36
NG_000006.1:g.33925G=
NG_059186.1:g.1412G=
NG_059271.1:g.5216G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.95+55G= MANE Select ENSP00000251595.6:n.95+55G=
ENST00000251595.10:c.95+55G= ENSP00000251595.6:n.95+55G=
ENST00000397806.1:c.-1-63G= ENSP00000380908.1:n.-1-63G=
ENST00000482565.1:n.169G=
ENST00000484216.1:n.64+55G=
NM_000517.4:c.95+55G= NP_000508.1:n.95+55G=
NM_000517.6:c.95+55G= MANE Select NP_000508.1:n.95+55G=