Canonical Allele Identifier: CA718603582

Gene: HBA2

Linked Data

• dbSNP Id: rs1210255063
• gnomAD v2: 16-223403-G-GTT
• gnomAD v3: 16-173404-G-GTT
• gnomAD v4: 16-173404-G-GTT
• MyVariant Identifiers: chr16:g.223403_223404insTT (hg19) ; chr16:g.173404_173405insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173404_173405insTT , CM000678.2:g.173404_173405insTT	GRCh38
NC_000016.9:g.223403_223404insTT , CM000678.1:g.223403_223404insTT	GRCh37
NC_000016.8:g.163403_163404insTT	NCBI36
NG_000006.1:g.34267_34268insTT
NG_059186.1:g.1754_1755insTT
NG_059271.1:g.5558_5559insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.301-68_301-67insTT MANE Select	ENSP00000251595.6:n.301-68_301-67insTT
ENST00000251595.10:c.301-68_301-67insTT	ENSP00000251595.6:n.301-68_301-67insTT
ENST00000397806.1:c.205-68_205-67insTT	ENSP00000380908.1:n.205-68_205-67insTT
ENST00000482565.1:n.437-68_437-67insTT
ENST00000484216.1:n.344_345insTT
NM_000517.4:c.301-68_301-67insTT	NP_000508.1:n.301-68_301-67insTT
NM_000517.6:c.301-68_301-67insTT MANE Select	NP_000508.1:n.301-68_301-67insTT