Canonical Allele Identifier: CA1949571487
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227078T= , CM000673.2:g.5227078T= GRCh38
NC_000011.9:g.5248308T= , CM000673.1:g.5248308T= GRCh37
NC_000011.8:g.5204884T= NCBI36
NG_000007.3:g.70538A=
NG_059281.1:g.4994A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-57A= ENSP00000494175.1:n.-57A=
ENST00000380315.2:c.-18-39A= ENSP00000369671.2:n.-18-39A=