Canonical Allele Identifier: CA2200882933
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176875A= , CM000678.2:g.176875A= GRCh38
NC_000016.9:g.226874A= , CM000678.1:g.226874A= GRCh37
NC_000016.8:g.166874A= NCBI36
NG_000006.1:g.37738A=
NG_059186.1:g.5225A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.96-54A= MANE Select ENSP00000322421.5:n.96-54A=
ENST00000397797.1:c.-1-54A= ENSP00000380899.1:n.-1-54A=
ENST00000472694.1:n.178A=
ENST00000487791.1:n.65-54A=
NM_000558.4:c.96-54A= NP_000549.1:n.96-54A=
NM_000558.5:c.96-54A= MANE Select NP_000549.1:n.96-54A=