Canonical Allele Identifier: CA2200882943
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1902150855
gnomAD v3: 16-176887-C-T
gnomAD v4: 16-176887-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176887C>T , CM000678.2:g.176887C>T GRCh38
NC_000016.9:g.226886C>T , CM000678.1:g.226886C>T GRCh37
NC_000016.8:g.166886C>T NCBI36
NG_000006.1:g.37750C>T
NG_059186.1:g.5237C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.96-42C>T MANE Select ENSP00000322421.5:n.96-42C>T
ENST00000397797.1:c.-1-42C>T ENSP00000380899.1:n.-1-42C>T
ENST00000472694.1:n.190C>T
ENST00000487791.1:n.65-42C>T
NM_000558.4:c.96-42C>T NP_000549.1:n.96-42C>T
NM_000558.5:c.96-42C>T MANE Select NP_000549.1:n.96-42C>T