Canonical Allele Identifier: CA2200882775
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176686C= , CM000678.2:g.176686C= GRCh38
NC_000016.9:g.226685C= , CM000678.1:g.226685C= GRCh37
NC_000016.8:g.166685C= NCBI36
NG_000006.1:g.37549C=
NG_059186.1:g.5036C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-31C= MANE Select ENSP00000322421.5:n.-31C=
NM_000558.4:c.-31C= NP_000549.1:n.-31C=
NM_000558.5:c.-31C= MANE Select NP_000549.1:n.-31C=