Canonical Allele Identifier: CA1949571475
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227072A= , CM000673.2:g.5227072A= GRCh38
NC_000011.9:g.5248302A= , CM000673.1:g.5248302A= GRCh37
NC_000011.8:g.5204878A= NCBI36
NG_000007.3:g.70544T=
NG_059281.1:g.5000T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-51T= ENSP00000494175.1:n.-51T=
ENST00000380315.2:c.-18-33T= ENSP00000369671.2:n.-18-33T=
ENST00000485743.1:n.1T=