Canonical Allele Identifier: CA718605757
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1256950782

Genomic Alleles

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

Transcript Alleles

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