Canonical Allele Identifier: CA393994954
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176760-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176760G>C , CM000678.2:g.176760G>C GRCh38
NC_000016.9:g.226759G>C , CM000678.1:g.226759G>C GRCh37
NC_000016.8:g.166759G>C NCBI36
NG_000006.1:g.37623G>C
NG_059186.1:g.5110G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.44G>C MANE Select ENSP00000322421.5:p.Trp15Ser
ENST00000397797.1:c.-4G>C ENSP00000380899.1:n.-4G>C
ENST00000472694.1:n.63G>C
ENST00000487791.1:n.13G>C
NM_000558.4:c.44G>C NP_000549.1:p.Trp15Ser
NM_000558.5:c.44G>C MANE Select NP_000549.1:p.Trp15Ser