Canonical Allele Identifier: CA2575852820
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173341-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173341G>T , CM000678.2:g.173341G>T GRCh38
NC_000016.9:g.223340G>T , CM000678.1:g.223340G>T GRCh37
NC_000016.8:g.163340G>T NCBI36
NG_000006.1:g.34204G>T
NG_059186.1:g.1691G>T
NG_059271.1:g.5495G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.300+12G>T MANE Select ENSP00000251595.6:n.300+12G>T
ENST00000251595.10:c.300+12G>T ENSP00000251595.6:n.300+12G>T
ENST00000397806.1:c.204+12G>T ENSP00000380908.1:n.204+12G>T
ENST00000482565.1:n.436+12G>T
ENST00000484216.1:n.281G>T
NM_000517.4:c.300+12G>T NP_000508.1:n.300+12G>T
NM_000517.6:c.300+12G>T MANE Select NP_000508.1:n.300+12G>T