Canonical Allele Identifier: CA2612161708
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5226181-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226181T>G , CM000673.2:g.5226181T>G GRCh38
NC_000011.9:g.5247411T>G , CM000673.1:g.5247411T>G GRCh37
NC_000011.8:g.5203987T>G NCBI36
NG_000007.3:g.71435A>C
NG_059281.1:g.5891A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+396A>C ENSP00000494175.1:n.315+396A>C
ENST00000335295.4:c.315+396A>C MANE Select ENSP00000333994.3:n.315+396A>C
ENST00000475226.1:n.247+396A>C
ENST00000633227.1:c.*131+396A>C ENSP00000488004.1:n.*131+396A>C
NM_000518.4:c.315+396A>C NP_000509.1:n.315+396A>C
NM_000518.5:c.315+396A>C MANE Select NP_000509.1:n.315+396A>C
Search 100 bp 5'
Search 100 bp 3'