Canonical Allele Identifier: CA2200883174
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177207G= , CM000678.2:g.177207G= GRCh38
NC_000016.9:g.227206G= , CM000678.1:g.227206G= GRCh37
NC_000016.8:g.167206G= NCBI36
NG_000006.1:g.38070G=
NG_059186.1:g.5557G=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.300+74G= MANE Select ENSP00000322421.5:n.300+74G=
ENST00000397797.1:c.204+74G= ENSP00000380899.1:n.204+74G=
ENST00000472694.1:n.436+74G=
ENST00000487791.1:n.343G=
NM_000558.4:c.300+74G= NP_000549.1:n.300+74G=
NM_000558.5:c.300+74G= MANE Select NP_000549.1:n.300+74G=