Canonical Allele Identifier: CA492994207
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.222968C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172969C>G , CM000678.2:g.172969C>G GRCh38
NC_000016.9:g.222968C>G , CM000678.1:g.222968C>G GRCh37
NC_000016.8:g.162968C>G NCBI36
NG_000006.1:g.33832C>G
NG_059186.1:g.1319C>G
NG_059271.1:g.5123C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.57C>G MANE Select ENSP00000251595.6:p.Gly19=
ENST00000251595.10:c.57C>G ENSP00000251595.6:p.Gly19=
ENST00000397806.1:c.-2+11C>G ENSP00000380908.1:n.-2+11C>G
ENST00000482565.1:n.76C>G
ENST00000484216.1:n.26C>G
NM_000517.4:c.57C>G NP_000508.1:p.Gly19=
NM_000517.6:c.57C>G MANE Select NP_000508.1:p.Gly19=
Search 100 bp 5'
Search 100 bp 3'