Canonical Allele Identifier: CA7770275
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs138407823
gnomAD v2: 16-227305-G-A
gnomAD v3: 16-177306-G-A
gnomAD v4: 16-177306-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177306G>A , CM000678.2:g.177306G>A GRCh38
NC_000016.9:g.227305G>A , CM000678.1:g.227305G>A GRCh37
NC_000016.8:g.167305G>A NCBI36
NG_000006.1:g.38169G>A
NG_059186.1:g.5656G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.324G>A MANE Select ENSP00000322421.5:p.Val108=
ENST00000397797.1:c.228G>A ENSP00000380899.1:p.Val76=
ENST00000472694.1:n.460G>A
NM_000558.4:c.324G>A NP_000549.1:p.Val108=
NM_000558.5:c.324G>A MANE Select NP_000549.1:p.Val108=