Canonical Allele Identifier: CA393993207
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173009-T-A
MyVariant Identifiers: chr16:g.223008T>A (hg19) chr16:g.173009T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173009T>A , CM000678.2:g.173009T>A GRCh38
NC_000016.9:g.223008T>A , CM000678.1:g.223008T>A GRCh37
NC_000016.8:g.163008T>A NCBI36
NG_000006.1:g.33872T>A
NG_059186.1:g.1359T>A
NG_059271.1:g.5163T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.95+2T>A MANE Select ENSP00000251595.6:n.95+2T>A
ENST00000251595.10:c.95+2T>A ENSP00000251595.6:n.95+2T>A
ENST00000397806.1:c.-2+51T>A ENSP00000380908.1:n.-2+51T>A
ENST00000482565.1:n.116T>A
ENST00000484216.1:n.64+2T>A
NM_000517.4:c.95+2T>A NP_000508.1:n.95+2T>A
NM_000517.6:c.95+2T>A MANE Select NP_000508.1:n.95+2T>A
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Search 100 bp 3'