Canonical Allele Identifier: CA2575852832
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173404G>T , CM000678.2:g.173404G>T GRCh38
NC_000016.9:g.223403G>T , CM000678.1:g.223403G>T GRCh37
NC_000016.8:g.163403G>T NCBI36
NG_000006.1:g.34267G>T
NG_059186.1:g.1754G>T
NG_059271.1:g.5558G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.301-68G>T MANE Select ENSP00000251595.6:n.301-68G>T
ENST00000251595.10:c.301-68G>T ENSP00000251595.6:n.301-68G>T
ENST00000397806.1:c.205-68G>T ENSP00000380908.1:n.205-68G>T
ENST00000482565.1:n.437-68G>T
ENST00000484216.1:n.344G>T
NM_000517.4:c.301-68G>T NP_000508.1:n.301-68G>T
NM_000517.6:c.301-68G>T MANE Select NP_000508.1:n.301-68G>T