Canonical Allele Identifier: CA2630736385
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-177427-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177427G>T , CM000678.2:g.177427G>T GRCh38
NC_000016.9:g.227426G>T , CM000678.1:g.227426G>T GRCh37
NC_000016.8:g.167426G>T NCBI36
NG_000006.1:g.38290G>T
NG_059186.1:g.5777G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.*16G>T MANE Select ENSP00000322421.5:n.*16G>T
ENST00000397797.1:c.*16G>T ENSP00000380899.1:n.*16G>T
ENST00000472694.1:n.581G>T
NM_000558.4:c.*16G>T NP_000549.1:n.*16G>T
NM_000558.5:c.*16G>T MANE Select NP_000549.1:n.*16G>T
Search 100 bp 5'
Search 100 bp 3'