Canonical Allele Identifier: CA2579829364
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227175T>A , CM000673.2:g.5227175T>A GRCh38
NC_000011.9:g.5248405T>A , CM000673.1:g.5248405T>A GRCh37
NC_000011.8:g.5204981T>A NCBI36
NG_000007.3:g.70441A>T
NG_059281.1:g.4897A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-154A>T ENSP00000494175.1:n.-154A>T
ENST00000380315.2:c.-18-136A>T ENSP00000369671.2:n.-18-136A>T