Canonical Allele Identifier: CA2612162211
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5225537-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225537A>C , CM000673.2:g.5225537A>C GRCh38
NC_000011.9:g.5246767A>C , CM000673.1:g.5246767A>C GRCh37
NC_000011.8:g.5203343A>C NCBI36
NG_000007.3:g.72079T>G
NG_059281.1:g.6535T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.*61T>G ENSP00000494175.1:n.*61T>G
ENST00000335295.4:c.*61T>G MANE Select ENSP00000333994.3:n.*61T>G
ENST00000633227.1:c.*321T>G ENSP00000488004.1:n.*321T>G
NM_000518.4:c.*61T>G NP_000509.1:n.*61T>G
NM_000518.5:c.*61T>G MANE Select NP_000509.1:n.*61T>G
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