Canonical Allele Identifier: CA393994259
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.223309T>A (hg19) chr16:g.173310T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173310T>A , CM000678.2:g.173310T>A GRCh38
NC_000016.9:g.223309T>A , CM000678.1:g.223309T>A GRCh37
NC_000016.8:g.163309T>A NCBI36
NG_000006.1:g.34173T>A
NG_059186.1:g.1660T>A
NG_059271.1:g.5464T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.281T>A MANE Select ENSP00000251595.6:p.Val94Glu
ENST00000251595.10:c.281T>A ENSP00000251595.6:p.Val94Glu
ENST00000397806.1:c.185T>A ENSP00000380908.1:p.Val62Glu
ENST00000482565.1:n.417T>A
ENST00000484216.1:n.250T>A
NM_000517.4:c.281T>A NP_000508.1:p.Val94Glu
NM_000517.6:c.281T>A MANE Select NP_000508.1:p.Val94Glu
Search 100 bp 5'
Search 100 bp 3'