Canonical Allele Identifier: CA2612162189
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5225519-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225519C>T , CM000673.2:g.5225519C>T GRCh38
NC_000011.9:g.5246749C>T , CM000673.1:g.5246749C>T GRCh37
NC_000011.8:g.5203325C>T NCBI36
NG_000007.3:g.72097G>A
NG_059281.1:g.6553G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*79G>A ENSP00000494175.1:n.*79G>A
ENST00000335295.4:c.*79G>A MANE Select ENSP00000333994.3:n.*79G>A
ENST00000633227.1:c.*339G>A ENSP00000488004.1:n.*339G>A
NM_000518.4:c.*79G>A NP_000509.1:n.*79G>A
NM_000518.5:c.*79G>A MANE Select NP_000509.1:n.*79G>A
Search 100 bp 5'
Search 100 bp 3'