Canonical Allele Identifier: CA125811
Gene: HBA1 HGNC NCBI
MyVariant.info:
GRCh38 chr16:g.177057A>C
GRCh37 chr16:g.227056A>C
Revel Score:
ENST00000320868 (MANE Select) 0.764
ENST00000397797 0.764
ClinVar RCV:
RCV000017095
ClinVar Variation:
15775
dbSNP:
33921047
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177057A>C , CM000678.2:g.177057A>C GRCh38
NC_000016.9:g.227056A>C , CM000678.1:g.227056A>C GRCh37
NC_000016.8:g.167056A>C NCBI36
NG_000006.1:g.37920A>C
NG_059186.1:g.5407A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.224A>C MANE Select ENSP00000322421.5:p.Asp75Ala
ENST00000397797.1:c.128A>C ENSP00000380899.1:p.Asp43Ala
ENST00000472694.1:n.360A>C
ENST00000487791.1:n.193A>C
NM_000558.4:c.224A>C NP_000549.1:p.Asp75Ala
NM_000558.5:c.224A>C MANE Select NP_000549.1:p.Asp75Ala
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