Canonical Allele Identifier: CA2200882806
Gene: HBA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176721T= , CM000678.2:g.176721T= GRCh38
NC_000016.9:g.226720T= , CM000678.1:g.226720T= GRCh37
NC_000016.8:g.166720T= NCBI36
NG_000006.1:g.37584T=
NG_059186.1:g.5071T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.5T= MANE Select ENSP00000322421.5:p.Val2=
ENST00000397797.1:c.-43T= ENSP00000380899.1:n.-43T=
ENST00000472694.1:n.24T=
NM_000558.4:c.5T= NP_000549.1:p.Val2=
NM_000558.5:c.5T= MANE Select NP_000549.1:p.Val2=
Search 100 bp 5'
Search 100 bp 3'