Canonical Allele Identifier: CA2200880925
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173516C= , CM000678.2:g.173516C= GRCh38
NC_000016.9:g.223515C= , CM000678.1:g.223515C= GRCh37
NC_000016.8:g.163515C= NCBI36
NG_000006.1:g.34379C=
NG_059186.1:g.1866C=
NG_059271.1:g.5670C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.345C= MANE Select ENSP00000251595.6:p.Pro115=
ENST00000251595.10:c.345C= ENSP00000251595.6:p.Pro115=
ENST00000397806.1:c.249C= ENSP00000380908.1:p.Pro83=
ENST00000482565.1:n.481C=
NM_000517.4:c.345C= NP_000508.1:p.Pro115=
NM_000517.6:c.345C= MANE Select NP_000508.1:p.Pro115=