Canonical Allele Identifier: CA934687297
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs1847519610
gnomAD v4: 11-5225508-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225508T>C , CM000673.2:g.5225508T>C GRCh38
NC_000011.9:g.5246738T>C , CM000673.1:g.5246738T>C GRCh37
NC_000011.8:g.5203314T>C NCBI36
NG_000007.3:g.72108A>G
NG_059281.1:g.6564A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*90A>G ENSP00000494175.1:n.*90A>G
ENST00000335295.4:c.*90A>G MANE Select ENSP00000333994.3:n.*90A>G
ENST00000633227.1:c.*350A>G ENSP00000488004.1:n.*350A>G
NM_000518.4:c.*90A>G NP_000509.1:n.*90A>G
NM_000518.5:c.*90A>G MANE Select NP_000509.1:n.*90A>G