Canonical Allele Identifier: CA393993405
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173183-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173183G>T , CM000678.2:g.173183G>T GRCh38
NC_000016.9:g.223182G>T , CM000678.1:g.223182G>T GRCh37
NC_000016.8:g.163182G>T NCBI36
NG_000006.1:g.34046G>T
NG_059186.1:g.1533G>T
NG_059271.1:g.5337G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.154G>T MANE Select ENSP00000251595.6:p.Gly52Cys
ENST00000251595.10:c.154G>T ENSP00000251595.6:p.Gly52Cys
ENST00000397806.1:c.58G>T ENSP00000380908.1:p.Gly20Cys
ENST00000482565.1:n.290G>T
ENST00000484216.1:n.123G>T
NM_000517.4:c.154G>T NP_000508.1:p.Gly52Cys
NM_000517.6:c.154G>T MANE Select NP_000508.1:p.Gly52Cys