Canonical Allele Identifier: CA7770227
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs63750090
gnomAD v2: 16-226759-G-A
gnomAD v4: 16-176760-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176760G>A , CM000678.2:g.176760G>A GRCh38
NC_000016.9:g.226759G>A , CM000678.1:g.226759G>A GRCh37
NC_000016.8:g.166759G>A NCBI36
NG_000006.1:g.37623G>A
NG_059186.1:g.5110G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.44G>A MANE Select ENSP00000322421.5:p.Trp15Ter
ENST00000397797.1:c.-4G>A ENSP00000380899.1:n.-4G>A
ENST00000472694.1:n.63G>A
ENST00000487791.1:n.13G>A
NM_000558.4:c.44G>A NP_000549.1:p.Trp15Ter
NM_000558.5:c.44G>A MANE Select NP_000549.1:p.Trp15Ter