Canonical Allele Identifier: CA973582116
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v3: 16-173447-C-CCTCG
gnomAD v4: 16-173447-C-CCTCG
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173447_173448insCTCG , CM000678.2:g.173447_173448insCTCG GRCh38
NC_000016.9:g.223446_223447insCTCG , CM000678.1:g.223446_223447insCTCG GRCh37
NC_000016.8:g.163446_163447insCTCG NCBI36
NG_000006.1:g.34310_34311insCTCG
NG_059186.1:g.1797_1798insCTCG
NG_059271.1:g.5601_5602insCTCG

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-25_301-24insCTCG MANE Select ENSP00000251595.6:n.301-25_301-24insCTCG
ENST00000251595.10:c.301-25_301-24insCTCG ENSP00000251595.6:n.301-25_301-24insCTCG
ENST00000397806.1:c.205-25_205-24insCTCG ENSP00000380908.1:n.205-25_205-24insCTCG
ENST00000482565.1:n.437-25_437-24insCTCG
ENST00000484216.1:n.387_388insCTCG
NM_000517.4:c.301-25_301-24insCTCG NP_000508.1:n.301-25_301-24insCTCG
NM_000517.6:c.301-25_301-24insCTCG MANE Select NP_000508.1:n.301-25_301-24insCTCG
Search 100 bp 5'
Search 100 bp 3'