Canonical Allele Identifier: CA2574735677
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5226879-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226879G>A , CM000673.2:g.5226879G>A GRCh38
NC_000011.9:g.5248109G>A , CM000673.1:g.5248109G>A GRCh37
NC_000011.8:g.5204685G>A NCBI36
NG_000007.3:g.70737C>T
NG_059281.1:g.5193C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.92+51C>T ENSP00000494175.1:n.92+51C>T
ENST00000335295.4:c.92+51C>T MANE Select ENSP00000333994.3:n.92+51C>T
ENST00000380315.2:c.92+51C>T ENSP00000369671.2:n.92+51C>T
ENST00000485743.1:n.143+51C>T
ENST00000633227.1:c.76+67C>T ENSP00000488004.1:n.76+67C>T
NM_000518.4:c.92+51C>T NP_000509.1:n.92+51C>T
NM_000518.5:c.92+51C>T MANE Select NP_000509.1:n.92+51C>T