Canonical Allele Identifier: CA2612162192
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5226493-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226493C>A , CM000673.2:g.5226493C>A GRCh38
NC_000011.9:g.5247723C>A , CM000673.1:g.5247723C>A GRCh37
NC_000011.8:g.5204299C>A NCBI36
NG_000007.3:g.71123G>T
NG_059281.1:g.5579G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+84G>T ENSP00000494175.1:n.315+84G>T
ENST00000335295.4:c.315+84G>T MANE Select ENSP00000333994.3:n.315+84G>T
ENST00000475226.1:n.247+84G>T
ENST00000485743.1:n.450G>T
ENST00000633227.1:c.*131+84G>T ENSP00000488004.1:n.*131+84G>T
NM_000518.4:c.315+84G>T NP_000509.1:n.315+84G>T
NM_000518.5:c.315+84G>T MANE Select NP_000509.1:n.315+84G>T