Canonical Allele Identifier: CA2579829255
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5227134-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227134T>A , CM000673.2:g.5227134T>A GRCh38
NC_000011.9:g.5248364T>A , CM000673.1:g.5248364T>A GRCh37
NC_000011.8:g.5204940T>A NCBI36
NG_000007.3:g.70482A>T
NG_059281.1:g.4938A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-113A>T ENSP00000494175.1:n.-113A>T
ENST00000380315.2:c.-18-95A>T ENSP00000369671.2:n.-18-95A>T