Canonical Allele Identifier: CA1949571577
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227100T= , CM000673.2:g.5227100T= GRCh38
NC_000011.9:g.5248330T= , CM000673.1:g.5248330T= GRCh37
NC_000011.8:g.5204906T= NCBI36
NG_000007.3:g.70516A=
NG_059281.1:g.4972A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380315.2:c.-18-61A= ENSP00000369671.2:n.-18-61A=
ENST00000647020.1:c.-79A= ENSP00000494175.1:n.-79A=