Canonical Allele Identifier: CA620161600
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs754685409
gnomAD v2: 16-226687-G-A
gnomAD v3: 16-176688-G-A
gnomAD v4: 16-176688-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176688G>A , CM000678.2:g.176688G>A GRCh38
NC_000016.9:g.226687G>A , CM000678.1:g.226687G>A GRCh37
NC_000016.8:g.166687G>A NCBI36
NG_000006.1:g.37551G>A
NG_059186.1:g.5038G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-29G>A MANE Select ENSP00000322421.5:n.-29G>A
NM_000558.4:c.-29G>A NP_000549.1:n.-29G>A
NM_000558.5:c.-29G>A MANE Select NP_000549.1:n.-29G>A