Canonical Allele Identifier: CA276417219
Gene: HBA1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177366G>T , CM000678.2:g.177366G>T GRCh38
NC_000016.9:g.227365G>T , CM000678.1:g.227365G>T GRCh37
NC_000016.8:g.167365G>T NCBI36
NG_000006.1:g.38229G>T
NG_059186.1:g.5716G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.384G>T MANE Select ENSP00000322421.5:p.Lys128Asn
ENST00000397797.1:c.288G>T ENSP00000380899.1:p.Lys96Asn
ENST00000472694.1:n.520G>T
NM_000558.4:c.384G>T NP_000549.1:p.Lys128Asn
NM_000558.5:c.384G>T MANE Select NP_000549.1:p.Lys128Asn