Canonical Allele Identifier: CA2579829269
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227138A>G , CM000673.2:g.5227138A>G GRCh38
NC_000011.9:g.5248368A>G , CM000673.1:g.5248368A>G GRCh37
NC_000011.8:g.5204944A>G NCBI36
NG_000007.3:g.70478T>C
NG_059281.1:g.4934T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-117T>C ENSP00000494175.1:n.-117T>C
ENST00000380315.2:c.-18-99T>C ENSP00000369671.2:n.-18-99T>C