Canonical Allele Identifier: CA2200882914
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176850C= , CM000678.2:g.176850C= GRCh38
NC_000016.9:g.226849C= , CM000678.1:g.226849C= GRCh37
NC_000016.8:g.166849C= NCBI36
NG_000006.1:g.37713C=
NG_059186.1:g.5200C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.95+39C= MANE Select ENSP00000322421.5:n.95+39C=
ENST00000397797.1:c.-1-79C= ENSP00000380899.1:n.-1-79C=
ENST00000472694.1:n.153C=
ENST00000487791.1:n.64+39C=
NM_000558.4:c.95+39C= NP_000549.1:n.95+39C=
NM_000558.5:c.95+39C= MANE Select NP_000549.1:n.95+39C=