Canonical Allele Identifier: CA7770167
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs756719608
ExAC: 16:223456 C / CGG
MyVariant Identifiers: chr16:g.223456_223457insGG (hg19) chr16:g.173457_173458insGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173457_173458insGG , CM000678.2:g.173457_173458insGG GRCh38
NC_000016.9:g.223456_223457insGG , CM000678.1:g.223456_223457insGG GRCh37
NC_000016.8:g.163456_163457insGG NCBI36
NG_000006.1:g.34320_34321insGG
NG_059186.1:g.1807_1808insGG
NG_059271.1:g.5611_5612insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.301-15_301-14insGG MANE Select ENSP00000251595.6:n.301-15_301-14insGG
ENST00000251595.10:c.301-15_301-14insGG ENSP00000251595.6:n.301-15_301-14insGG
ENST00000397806.1:c.205-15_205-14insGG ENSP00000380908.1:n.205-15_205-14insGG
ENST00000482565.1:n.437-15_437-14insGG
ENST00000484216.1:n.397_398insGG
NM_000517.4:c.301-15_301-14insGG NP_000508.1:n.301-15_301-14insGG
NM_000517.6:c.301-15_301-14insGG MANE Select NP_000508.1:n.301-15_301-14insGG
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