Canonical Allele Identifier: CA276414509
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs63750030
MyVariant Identifiers: chr16:g.223061G>A (hg19) chr16:g.173062G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173062G>A , CM000678.2:g.173062G>A GRCh38
NC_000016.9:g.223061G>A , CM000678.1:g.223061G>A GRCh37
NC_000016.8:g.163061G>A NCBI36
NG_000006.1:g.33925G>A
NG_059186.1:g.1412G>A
NG_059271.1:g.5216G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.95+55G>A MANE Select ENSP00000251595.6:n.95+55G>A
ENST00000251595.10:c.95+55G>A ENSP00000251595.6:n.95+55G>A
ENST00000397806.1:c.-1-63G>A ENSP00000380908.1:n.-1-63G>A
ENST00000482565.1:n.169G>A
ENST00000484216.1:n.64+55G>A
NM_000517.4:c.95+55G>A NP_000508.1:n.95+55G>A
NM_000517.6:c.95+55G>A MANE Select NP_000508.1:n.95+55G>A
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