Canonical Allele Identifier: CA492994519
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.223133G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173134G>C , CM000678.2:g.173134G>C GRCh38
NC_000016.9:g.223133G>C , CM000678.1:g.223133G>C GRCh37
NC_000016.8:g.163133G>C NCBI36
NG_000006.1:g.33997G>C
NG_059186.1:g.1484G>C
NG_059271.1:g.5288G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.105G>C MANE Select ENSP00000251595.6:p.Leu35=
ENST00000251595.10:c.105G>C ENSP00000251595.6:p.Leu35=
ENST00000397806.1:c.9G>C ENSP00000380908.1:p.Leu3=
ENST00000482565.1:n.241G>C
ENST00000484216.1:n.74G>C
NM_000517.4:c.105G>C NP_000508.1:p.Leu35=
NM_000517.6:c.105G>C MANE Select NP_000508.1:p.Leu35=
Search 100 bp 5'
Search 100 bp 3'