Canonical Allele Identifier: CA2200882807
Gene: HBA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176722G= , CM000678.2:g.176722G= GRCh38
NC_000016.9:g.226721G= , CM000678.1:g.226721G= GRCh37
NC_000016.8:g.166721G= NCBI36
NG_000006.1:g.37585G=
NG_059186.1:g.5072G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.6G= MANE Select ENSP00000322421.5:p.Val2=
ENST00000397797.1:c.-42G= ENSP00000380899.1:n.-42G=
ENST00000472694.1:n.25G=
NM_000558.4:c.6G= NP_000549.1:p.Val2=
NM_000558.5:c.6G= MANE Select NP_000549.1:p.Val2=
Search 100 bp 5'
Search 100 bp 3'