Canonical Allele Identifier: CA2200880855
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1567163587
gnomAD v4: 16-173430-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173430C>T , CM000678.2:g.173430C>T GRCh38
NC_000016.9:g.223429C>T , CM000678.1:g.223429C>T GRCh37
NC_000016.8:g.163429C>T NCBI36
NG_000006.1:g.34293C>T
NG_059186.1:g.1780C>T
NG_059271.1:g.5584C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-42C>T MANE Select ENSP00000251595.6:n.301-42C>T
ENST00000251595.10:c.301-42C>T ENSP00000251595.6:n.301-42C>T
ENST00000397806.1:c.205-42C>T ENSP00000380908.1:n.205-42C>T
ENST00000482565.1:n.437-42C>T
ENST00000484216.1:n.370C>T
NM_000517.4:c.301-42C>T NP_000508.1:n.301-42C>T
NM_000517.6:c.301-42C>T MANE Select NP_000508.1:n.301-42C>T