Canonical Allele Identifier: CA1949571832
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227176G= , CM000673.2:g.5227176G= GRCh38
NC_000011.9:g.5248406G= , CM000673.1:g.5248406G= GRCh37
NC_000011.8:g.5204982G= NCBI36
NG_000007.3:g.70440C=
NG_059281.1:g.4896C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-155C= ENSP00000494175.1:n.-155C=
ENST00000380315.2:c.-18-137C= ENSP00000369671.2:n.-18-137C=