Canonical Allele Identifier: CA2731571764
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs376827361
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177430A>C , CM000678.2:g.177430A>C GRCh38
NC_000016.9:g.227429A>C , CM000678.1:g.227429A>C GRCh37
NC_000016.8:g.167429A>C NCBI36
NG_000006.1:g.38293A>C
NG_059186.1:g.5780A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.*19A>C MANE Select ENSP00000322421.5:n.*19A>C
ENST00000397797.1:c.*19A>C ENSP00000380899.1:n.*19A>C
ENST00000472694.1:n.584A>C
NM_000558.4:c.*19A>C NP_000549.1:n.*19A>C
NM_000558.5:c.*19A>C MANE Select NP_000549.1:n.*19A>C
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