Canonical Allele Identifier: CA2630738713
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176680-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176680A>G , CM000678.2:g.176680A>G GRCh38
NC_000016.9:g.226679A>G , CM000678.1:g.226679A>G GRCh37
NC_000016.8:g.166679A>G NCBI36
NG_000006.1:g.37543A>G
NG_059186.1:g.5030A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-37A>G MANE Select ENSP00000322421.5:n.-37A>G
NM_000558.4:c.-37A>G NP_000549.1:n.-37A>G
NM_000558.5:c.-37A>G MANE Select NP_000549.1:n.-37A>G
Search 100 bp 5'
Search 100 bp 3'