Canonical Allele Identifier: CA2579829322
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5227156-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227156A>G , CM000673.2:g.5227156A>G GRCh38
NC_000011.9:g.5248386A>G , CM000673.1:g.5248386A>G GRCh37
NC_000011.8:g.5204962A>G NCBI36
NG_000007.3:g.70460T>C
NG_059281.1:g.4916T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-135T>C ENSP00000494175.1:n.-135T>C
ENST00000380315.2:c.-18-117T>C ENSP00000369671.2:n.-18-117T>C