Canonical Allele Identifier: CA620304409
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs753869946
gnomAD v2: 16-223426-C-T
gnomAD v4: 16-173427-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173427C>T , CM000678.2:g.173427C>T GRCh38
NC_000016.9:g.223426C>T , CM000678.1:g.223426C>T GRCh37
NC_000016.8:g.163426C>T NCBI36
NG_000006.1:g.34290C>T
NG_059186.1:g.1777C>T
NG_059271.1:g.5581C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-45C>T MANE Select ENSP00000251595.6:n.301-45C>T
ENST00000251595.10:c.301-45C>T ENSP00000251595.6:n.301-45C>T
ENST00000397806.1:c.205-45C>T ENSP00000380908.1:n.205-45C>T
ENST00000482565.1:n.437-45C>T
ENST00000484216.1:n.367C>T
NM_000517.4:c.301-45C>T NP_000508.1:n.301-45C>T
NM_000517.6:c.301-45C>T MANE Select NP_000508.1:n.301-45C>T