Canonical Allele Identifier: CA393993513
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173217-T-G
MyVariant Identifiers: chr16:g.223216T>G (hg19) chr16:g.173217T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173217T>G , CM000678.2:g.173217T>G GRCh38
NC_000016.9:g.223216T>G , CM000678.1:g.223216T>G GRCh37
NC_000016.8:g.163216T>G NCBI36
NG_000006.1:g.34080T>G
NG_059186.1:g.1567T>G
NG_059271.1:g.5371T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.188T>G MANE Select ENSP00000251595.6:p.Val63Gly
ENST00000251595.10:c.188T>G ENSP00000251595.6:p.Val63Gly
ENST00000397806.1:c.92T>G ENSP00000380908.1:p.Val31Gly
ENST00000482565.1:n.324T>G
ENST00000484216.1:n.157T>G
NM_000517.4:c.188T>G NP_000508.1:p.Val63Gly
NM_000517.6:c.188T>G MANE Select NP_000508.1:p.Val63Gly
Search 100 bp 5'
Search 100 bp 3'