Canonical Allele Identifier: CA2200883310
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177386C= , CM000678.2:g.177386C= GRCh38
NC_000016.9:g.227385C= , CM000678.1:g.227385C= GRCh37
NC_000016.8:g.167385C= NCBI36
NG_000006.1:g.38249C=
NG_059186.1:g.5736C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.404C= MANE Select ENSP00000322421.5:p.Thr135=
ENST00000397797.1:c.308C= ENSP00000380899.1:p.Thr103=
ENST00000472694.1:n.540C=
NM_000558.4:c.404C= NP_000549.1:p.Thr135=
NM_000558.5:c.404C= MANE Select NP_000549.1:p.Thr135=