Canonical Allele Identifier: CA1949571568
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227099T= , CM000673.2:g.5227099T= GRCh38
NC_000011.9:g.5248329T= , CM000673.1:g.5248329T= GRCh37
NC_000011.8:g.5204905T= NCBI36
NG_000007.3:g.70517A=
NG_059281.1:g.4973A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-78A= ENSP00000494175.1:n.-78A=
ENST00000380315.2:c.-18-60A= ENSP00000369671.2:n.-18-60A=