Canonical Allele Identifier: CA1949570152
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226925C= , CM000673.2:g.5226925C= GRCh38
NC_000011.9:g.5248155C= , CM000673.1:g.5248155C= GRCh37
NC_000011.8:g.5204731C= NCBI36
NG_000007.3:g.70691G=
NG_059281.1:g.5147G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.92+5G= ENSP00000494175.1:n.92+5G=
ENST00000335295.4:c.92+5G= MANE Select ENSP00000333994.3:n.92+5G=
ENST00000380315.2:c.92+5G= ENSP00000369671.2:n.92+5G=
ENST00000485743.1:n.143+5G=
ENST00000633227.1:c.76+21G= ENSP00000488004.1:n.76+21G=
NM_000518.4:c.92+5G= NP_000509.1:n.92+5G=
NM_000518.5:c.92+5G= MANE Select NP_000509.1:n.92+5G=