Canonical Allele Identifier: CA276415462
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs33972894
gnomAD v4: 16-173555-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173555G>C , CM000678.2:g.173555G>C GRCh38
NC_000016.9:g.223554G>C , CM000678.1:g.223554G>C GRCh37
NC_000016.8:g.163554G>C NCBI36
NG_000006.1:g.34418G>C
NG_059186.1:g.1905G>C
NG_059271.1:g.5709G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.384G>C MANE Select ENSP00000251595.6:p.Lys128Asn
ENST00000251595.10:c.384G>C ENSP00000251595.6:p.Lys128Asn
ENST00000397806.1:c.288G>C ENSP00000380908.1:p.Lys96Asn
ENST00000482565.1:n.520G>C
NM_000517.4:c.384G>C NP_000508.1:p.Lys128Asn
NM_000517.6:c.384G>C MANE Select NP_000508.1:p.Lys128Asn