Canonical Allele Identifier: CA718603602

Gene: HBA2

Linked Data

• dbSNP Id: rs1466371898
• gnomAD v3: 16-173441-C-T
• gnomAD v4: 16-173441-C-T
• MyVariant Identifiers: chr16:g.223440C>T (hg19) ; chr16:g.173441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173441C>T , CM000678.2:g.173441C>T	GRCh38
NC_000016.9:g.223440C>T , CM000678.1:g.223440C>T	GRCh37
NC_000016.8:g.163440C>T	NCBI36
NG_000006.1:g.34304C>T
NG_059186.1:g.1791C>T
NG_059271.1:g.5595C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.301-31C>T MANE Select	ENSP00000251595.6:n.301-31C>T
ENST00000251595.10:c.301-31C>T	ENSP00000251595.6:n.301-31C>T
ENST00000397806.1:c.205-31C>T	ENSP00000380908.1:n.205-31C>T
ENST00000482565.1:n.437-31C>T
ENST00000484216.1:n.381C>T
NM_000517.4:c.301-31C>T	NP_000508.1:n.301-31C>T
NM_000517.6:c.301-31C>T MANE Select	NP_000508.1:n.301-31C>T