Canonical Allele Identifier: CA1139532153
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173449_173450insTCGGCCCC , CM000678.2:g.173449_173450insTCGGCCCC GRCh38
NC_000016.9:g.223448_223449insTCGGCCCC , CM000678.1:g.223448_223449insTCGGCCCC GRCh37
NC_000016.8:g.163448_163449insTCGGCCCC NCBI36
NG_000006.1:g.34312_34313insTCGGCCCC
NG_059186.1:g.1799_1800insTCGGCCCC
NG_059271.1:g.5603_5604insTCGGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.301-23_301-22insTCGGCCCC MANE Select ENSP00000251595.6:n.301-23_301-22insTCGGCCCC
ENST00000251595.10:c.301-23_301-22insTCGGCCCC ENSP00000251595.6:n.301-23_301-22insTCGGCCCC
ENST00000397806.1:c.205-23_205-22insTCGGCCCC ENSP00000380908.1:n.205-23_205-22insTCGGCCCC
ENST00000482565.1:n.437-23_437-22insTCGGCCCC
ENST00000484216.1:n.389_390insTCGGCCCC
NM_000517.4:c.301-23_301-22insTCGGCCCC NP_000508.1:n.301-23_301-22insTCGGCCCC
NM_000517.6:c.301-23_301-22insTCGGCCCC MANE Select NP_000508.1:n.301-23_301-22insTCGGCCCC
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