Canonical Allele Identifier: CA973582688

Gene: HBA2

Linked Data

• dbSNP Id: rs1902066913

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173642C>G , CM000678.2:g.173642C>G	GRCh38
NC_000016.9:g.223641C>G , CM000678.1:g.223641C>G	GRCh37
NC_000016.8:g.163641C>G	NCBI36
NG_000006.1:g.34505C>G
NG_059186.1:g.1992C>G
NG_059271.1:g.5796C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.*42C>G MANE Select	ENSP00000251595.6:n.*42C>G
ENST00000251595.10:c.*42C>G	ENSP00000251595.6:n.*42C>G
ENST00000397806.1:c.*42C>G	ENSP00000380908.1:n.*42C>G
ENST00000482565.1:n.607C>G
NM_000517.4:c.*42C>G	NP_000508.1:n.*42C>G
NM_000517.6:c.*42C>G MANE Select	NP_000508.1:n.*42C>G