Canonical Allele Identifier: CA2630739385
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176873-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176873T>A , CM000678.2:g.176873T>A GRCh38
NC_000016.9:g.226872T>A , CM000678.1:g.226872T>A GRCh37
NC_000016.8:g.166872T>A NCBI36
NG_000006.1:g.37736T>A
NG_059186.1:g.5223T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.96-56T>A MANE Select ENSP00000322421.5:n.96-56T>A
ENST00000397797.1:c.-1-56T>A ENSP00000380899.1:n.-1-56T>A
ENST00000472694.1:n.176T>A
ENST00000487791.1:n.65-56T>A
NM_000558.4:c.96-56T>A NP_000549.1:n.96-56T>A
NM_000558.5:c.96-56T>A MANE Select NP_000549.1:n.96-56T>A
Search 100 bp 5'
Search 100 bp 3'