Canonical Allele Identifier: CA2200880794
Gene: HBA2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173335C= , CM000678.2:g.173335C= GRCh38
NC_000016.9:g.223334C= , CM000678.1:g.223334C= GRCh37
NC_000016.8:g.163334C= NCBI36
NG_000006.1:g.34198C=
NG_059186.1:g.1685C=
NG_059271.1:g.5489C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.300+6C= MANE Select ENSP00000251595.6:n.300+6C=
ENST00000251595.10:c.300+6C= ENSP00000251595.6:n.300+6C=
ENST00000397806.1:c.204+6C= ENSP00000380908.1:n.204+6C=
ENST00000482565.1:n.436+6C=
ENST00000484216.1:n.275C=
NM_000517.4:c.300+6C= NP_000508.1:n.300+6C=
NM_000517.6:c.300+6C= MANE Select NP_000508.1:n.300+6C=
Search 100 bp 5'
Search 100 bp 3'