Canonical Allele Identifier: CA2200882786
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176696C= , CM000678.2:g.176696C= GRCh38
NC_000016.9:g.226695C= , CM000678.1:g.226695C= GRCh37
NC_000016.8:g.166695C= NCBI36
NG_000006.1:g.37559C=
NG_059186.1:g.5046C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-21C= MANE Select ENSP00000322421.5:n.-21C=
NM_000558.4:c.-21C= NP_000549.1:n.-21C=
NM_000558.5:c.-21C= MANE Select NP_000549.1:n.-21C=