Canonical Allele Identifier: CA393994953
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176759T>G , CM000678.2:g.176759T>G GRCh38
NC_000016.9:g.226758T>G , CM000678.1:g.226758T>G GRCh37
NC_000016.8:g.166758T>G NCBI36
NG_000006.1:g.37622T>G
NG_059186.1:g.5109T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.43T>G MANE Select ENSP00000322421.5:p.Trp15Gly
ENST00000397797.1:c.-5T>G ENSP00000380899.1:n.-5T>G
ENST00000472694.1:n.62T>G
ENST00000487791.1:n.12T>G
NM_000558.4:c.43T>G NP_000549.1:p.Trp15Gly
NM_000558.5:c.43T>G MANE Select NP_000549.1:p.Trp15Gly