Canonical Allele Identifier: CA2612162269
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5226841-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226841G>T , CM000673.2:g.5226841G>T GRCh38
NC_000011.9:g.5248071G>T , CM000673.1:g.5248071G>T GRCh37
NC_000011.8:g.5204647G>T NCBI36
NG_000007.3:g.70775C>A
NG_059281.1:g.5231C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.93-42C>A ENSP00000494175.1:n.93-42C>A
ENST00000335295.4:c.93-42C>A MANE Select ENSP00000333994.3:n.93-42C>A
ENST00000380315.2:c.93-42C>A ENSP00000369671.2:n.93-42C>A
ENST00000485743.1:n.144-42C>A
ENST00000633227.1:c.77-42C>A ENSP00000488004.1:n.77-42C>A
NM_000518.4:c.93-42C>A NP_000509.1:n.93-42C>A
NM_000518.5:c.93-42C>A MANE Select NP_000509.1:n.93-42C>A
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