Canonical Allele Identifier: CA276416446
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs281860646

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176752G>T , CM000678.2:g.176752G>T GRCh38
NC_000016.9:g.226751G>T , CM000678.1:g.226751G>T GRCh37
NC_000016.8:g.166751G>T NCBI36
NG_000006.1:g.37615G>T
NG_059186.1:g.5102G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.36G>T MANE Select ENSP00000322421.5:p.Lys12Asn
ENST00000397797.1:c.-12G>T ENSP00000380899.1:n.-12G>T
ENST00000472694.1:n.55G>T
ENST00000487791.1:n.5G>T
NM_000558.4:c.36G>T NP_000549.1:p.Lys12Asn
NM_000558.5:c.36G>T MANE Select NP_000549.1:p.Lys12Asn