Canonical Allele Identifier: CA620161602
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1216560017
gnomAD v2: 16-226691-C-G
gnomAD v4: 16-176692-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176692C>G , CM000678.2:g.176692C>G GRCh38
NC_000016.9:g.226691C>G , CM000678.1:g.226691C>G GRCh37
NC_000016.8:g.166691C>G NCBI36
NG_000006.1:g.37555C>G
NG_059186.1:g.5042C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-25C>G MANE Select ENSP00000322421.5:n.-25C>G
NM_000558.4:c.-25C>G NP_000549.1:n.-25C>G
NM_000558.5:c.-25C>G MANE Select NP_000549.1:n.-25C>G