Canonical Allele Identifier: CA2200882974
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176926C= , CM000678.2:g.176926C= GRCh38
NC_000016.9:g.226925C= , CM000678.1:g.226925C= GRCh37
NC_000016.8:g.166925C= NCBI36
NG_000006.1:g.37789C=
NG_059186.1:g.5276C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.96-3C= MANE Select ENSP00000322421.5:n.96-3C=
ENST00000397797.1:c.-1-3C= ENSP00000380899.1:n.-1-3C=
ENST00000472694.1:n.229C=
ENST00000487791.1:n.65-3C=
NM_000558.4:c.96-3C= NP_000549.1:n.96-3C=
NM_000558.5:c.96-3C= MANE Select NP_000549.1:n.96-3C=