Canonical Allele Identifier: CA393994951
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176757C>G , CM000678.2:g.176757C>G GRCh38
NC_000016.9:g.226756C>G , CM000678.1:g.226756C>G GRCh37
NC_000016.8:g.166756C>G NCBI36
NG_000006.1:g.37620C>G
NG_059186.1:g.5107C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.41C>G MANE Select ENSP00000322421.5:p.Ala14Gly
ENST00000397797.1:c.-7C>G ENSP00000380899.1:n.-7C>G
ENST00000472694.1:n.60C>G
ENST00000487791.1:n.10C>G
NM_000558.4:c.41C>G NP_000549.1:p.Ala14Gly
NM_000558.5:c.41C>G MANE Select NP_000549.1:p.Ala14Gly