Canonical Allele Identifier: CA2579829487
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5227050-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227050C>G , CM000673.2:g.5227050C>G GRCh38
NC_000011.9:g.5248280C>G , CM000673.1:g.5248280C>G GRCh37
NC_000011.8:g.5204856C>G NCBI36
NG_000007.3:g.70566G>C
NG_059281.1:g.5022G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-29G>C ENSP00000494175.1:n.-29G>C
ENST00000335295.4:c.-29G>C MANE Select ENSP00000333994.3:n.-29G>C
ENST00000380315.2:c.-18-11G>C ENSP00000369671.2:n.-18-11G>C
ENST00000485743.1:n.23G>C
ENST00000633227.1:c.-29G>C ENSP00000488004.1:n.-29G>C
NM_000518.4:c.-29G>C NP_000509.1:n.-29G>C
NM_000518.5:c.-29G>C MANE Select NP_000509.1:n.-29G>C
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