Canonical Allele Identifier: CA1949595891

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5281833G= , CM000673.2:g.5281833G= GRCh38
NC_000011.9:g.5303063G= , CM000673.1:g.5303063G= GRCh37
NC_000011.8:g.5259639G= NCBI36
NG_000007.3:g.15783C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000292896.3:c.-266-11677C= (HBE1) ENSP00000292896.2:n.-266-11677C=
ENST00000380252.6:c.-73-27319C= (HBG2) ENSP00000369602.2:n.-73-27319C=
ENST00000380259.7:c.1110-26668C= ENSP00000369609.3:n.1110-26668C=
ENST00000643199.1:n.90-11677C=
ENST00000646569.1:n.59-22296C=
ENST00000380237.5:c.-267+76C= (HBE1) ENSP00000369586.1:n.-267+76C=
ENST00000380252.5:c.63-27319C= (HBG2) ENSP00000369602.1:n.63-27319C=
ENST00000380259.6:c.-437-26668C= (HBG2) ENSP00000369609.2:n.-437-26668C=
ENST00000396895.1:c.-266-11677C= (HBE1) ENSP00000380104.1:n.-266-11677C=
XM_011520036.1:c.-355+76C= (HBE1) XP_011518338.1:n.-355+76C=