Canonical Allele Identifier: CA393994942
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176751A>C , CM000678.2:g.176751A>C GRCh38
NC_000016.9:g.226750A>C , CM000678.1:g.226750A>C GRCh37
NC_000016.8:g.166750A>C NCBI36
NG_000006.1:g.37614A>C
NG_059186.1:g.5101A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.35A>C MANE Select ENSP00000322421.5:p.Lys12Thr
ENST00000397797.1:c.-13A>C ENSP00000380899.1:n.-13A>C
ENST00000472694.1:n.54A>C
ENST00000487791.1:n.4A>C
NM_000558.4:c.35A>C NP_000549.1:p.Lys12Thr
NM_000558.5:c.35A>C MANE Select NP_000549.1:p.Lys12Thr