Canonical Allele Identifier: CA2731773154
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs2142018516

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173607G>T , CM000678.2:g.173607G>T GRCh38
NC_000016.9:g.223606G>T , CM000678.1:g.223606G>T GRCh37
NC_000016.8:g.163606G>T NCBI36
NG_000006.1:g.34470G>T
NG_059186.1:g.1957G>T
NG_059271.1:g.5761G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.*7G>T MANE Select ENSP00000251595.6:n.*7G>T
ENST00000251595.10:c.*7G>T ENSP00000251595.6:n.*7G>T
ENST00000397806.1:c.*7G>T ENSP00000380908.1:n.*7G>T
ENST00000482565.1:n.572G>T
NM_000517.4:c.*7G>T NP_000508.1:n.*7G>T
NM_000517.6:c.*7G>T MANE Select NP_000508.1:n.*7G>T