Canonical Allele Identifier: CA2580084026
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 2103192
ClinVar RCV Id: RCV003022016
gnomAD v4: 11-5226920-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226920T>G , CM000673.2:g.5226920T>G GRCh38
NC_000011.9:g.5248150T>G , CM000673.1:g.5248150T>G GRCh37
NC_000011.8:g.5204726T>G NCBI36
NG_000007.3:g.70696A>C
NG_059281.1:g.5152A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.92+10A>C ENSP00000494175.1:n.92+10A>C
ENST00000335295.4:c.92+10A>C MANE Select ENSP00000333994.3:n.92+10A>C
ENST00000380315.2:c.92+10A>C ENSP00000369671.2:n.92+10A>C
ENST00000485743.1:n.143+10A>C
ENST00000633227.1:c.76+26A>C ENSP00000488004.1:n.76+26A>C
NM_000518.4:c.92+10A>C NP_000509.1:n.92+10A>C
NM_000518.5:c.92+10A>C MANE Select NP_000509.1:n.92+10A>C
Search 100 bp 5'
Search 100 bp 3'