Canonical Allele Identifier: CA393994941
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.35A>T MANE Select ENSP00000322421.5:p.Lys12Met
ENST00000397797.1:c.-13A>T ENSP00000380899.1:n.-13A>T
ENST00000472694.1:n.54A>T
ENST00000487791.1:n.4A>T
NM_000558.4:c.35A>T NP_000549.1:p.Lys12Met
NM_000558.5:c.35A>T MANE Select NP_000549.1:p.Lys12Met