Canonical Allele Identifier: CA2723203606
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs2133588983

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226842C>A , CM000673.2:g.5226842C>A GRCh38
NC_000011.9:g.5248072C>A , CM000673.1:g.5248072C>A GRCh37
NC_000011.8:g.5204648C>A NCBI36
NG_000007.3:g.70774G>T
NG_059281.1:g.5230G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.93-43G>T ENSP00000494175.1:n.93-43G>T
ENST00000335295.4:c.93-43G>T MANE Select ENSP00000333994.3:n.93-43G>T
ENST00000380315.2:c.93-43G>T ENSP00000369671.2:n.93-43G>T
ENST00000485743.1:n.144-43G>T
ENST00000633227.1:c.77-43G>T ENSP00000488004.1:n.77-43G>T
NM_000518.4:c.93-43G>T NP_000509.1:n.93-43G>T
NM_000518.5:c.93-43G>T MANE Select NP_000509.1:n.93-43G>T