Canonical Allele Identifier: CA2630738739
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176696-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176696C>A , CM000678.2:g.176696C>A GRCh38
NC_000016.9:g.226695C>A , CM000678.1:g.226695C>A GRCh37
NC_000016.8:g.166695C>A NCBI36
NG_000006.1:g.37559C>A
NG_059186.1:g.5046C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-21C>A MANE Select ENSP00000322421.5:n.-21C>A
NM_000558.4:c.-21C>A NP_000549.1:n.-21C>A
NM_000558.5:c.-21C>A MANE Select NP_000549.1:n.-21C>A
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