Canonical Allele Identifier: CA2630737130
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173062-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173062G>T , CM000678.2:g.173062G>T GRCh38
NC_000016.9:g.223061G>T , CM000678.1:g.223061G>T GRCh37
NC_000016.8:g.163061G>T NCBI36
NG_000006.1:g.33925G>T
NG_059186.1:g.1412G>T
NG_059271.1:g.5216G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.95+55G>T MANE Select ENSP00000251595.6:n.95+55G>T
ENST00000251595.10:c.95+55G>T ENSP00000251595.6:n.95+55G>T
ENST00000397806.1:c.-1-63G>T ENSP00000380908.1:n.-1-63G>T
ENST00000482565.1:n.169G>T
ENST00000484216.1:n.64+55G>T
NM_000517.4:c.95+55G>T NP_000508.1:n.95+55G>T
NM_000517.6:c.95+55G>T MANE Select NP_000508.1:n.95+55G>T