Canonical Allele Identifier: CA393995777
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177293A>T , CM000678.2:g.177293A>T GRCh38
NC_000016.9:g.227292A>T , CM000678.1:g.227292A>T GRCh37
NC_000016.8:g.167292A>T NCBI36
NG_000006.1:g.38156A>T
NG_059186.1:g.5643A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.311A>T MANE Select ENSP00000322421.5:p.His104Leu
ENST00000397797.1:c.215A>T ENSP00000380899.1:p.His72Leu
ENST00000472694.1:n.447A>T
NM_000558.4:c.311A>T NP_000549.1:p.His104Leu
NM_000558.5:c.311A>T MANE Select NP_000549.1:p.His104Leu