Canonical Allele Identifier: CA2574735562
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5225564-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225564C>A , CM000673.2:g.5225564C>A GRCh38
NC_000011.9:g.5246794C>A , CM000673.1:g.5246794C>A GRCh37
NC_000011.8:g.5203370C>A NCBI36
NG_000007.3:g.72052G>T
NG_059281.1:g.6508G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*34G>T ENSP00000494175.1:n.*34G>T
ENST00000335295.4:c.*34G>T MANE Select ENSP00000333994.3:n.*34G>T
ENST00000633227.1:c.*294G>T ENSP00000488004.1:n.*294G>T
NM_000518.4:c.*34G>T NP_000509.1:n.*34G>T
NM_000518.5:c.*34G>T MANE Select NP_000509.1:n.*34G>T