Canonical Allele Identifier: CA2589876424
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs2142017782
gnomAD v3: 16-173064-C-T
gnomAD v4: 16-173064-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173064C>T , CM000678.2:g.173064C>T GRCh38
NC_000016.9:g.223063C>T , CM000678.1:g.223063C>T GRCh37
NC_000016.8:g.163063C>T NCBI36
NG_000006.1:g.33927C>T
NG_059186.1:g.1414C>T
NG_059271.1:g.5218C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.95+57C>T MANE Select ENSP00000251595.6:n.95+57C>T
ENST00000251595.10:c.95+57C>T ENSP00000251595.6:n.95+57C>T
ENST00000397806.1:c.-1-61C>T ENSP00000380908.1:n.-1-61C>T
ENST00000482565.1:n.171C>T
ENST00000484216.1:n.64+57C>T
NM_000517.4:c.95+57C>T NP_000508.1:n.95+57C>T
NM_000517.6:c.95+57C>T MANE Select NP_000508.1:n.95+57C>T