Canonical Allele Identifier: CA2838473507

Gene: HBE1 HBG2 OR51B5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5398357T>C , CM000673.2:g.5398357T>C	GRCh38
NC_000011.9:g.5419587T>C , CM000673.1:g.5419587T>C	GRCh37
NC_000011.8:g.5376163T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292896.3:c.-267+107212A>G (HBE1)	ENSP00000292896.2:n.-267+107212A>G
ENST00000380252.6:c.-74+106994A>G (HBG2)	ENSP00000369602.2:n.-74+106994A>G
ENST00000380259.7:c.983-52458A>G	ENSP00000369609.3:n.983-52458A>G
ENST00000415970.6:n.85-51447A>G (OR51B5)
ENST00000418729.1:n.85-51447A>G (OR51B5)
ENST00000420465.6:n.46-51447A>G (OR51B5)
ENST00000420726.6:n.46-51447A>G (OR51B5)
ENST00000380237.5:c.-310+107212A>G (HBE1)	ENSP00000369586.1:n.-310+107212A>G
ENST00000380252.5:c.62+106994A>G (HBG2)	ENSP00000369602.1:n.62+106994A>G
ENST00000380259.6:c.-564-52458A>G (HBG2)	ENSP00000369609.2:n.-564-52458A>G
ENST00000396895.1:c.-267+107212A>G (HBE1)	ENSP00000380104.1:n.-267+107212A>G
NM_001005567.2:c.-359-51447A>G (OR51B5)	NP_001005567.2:n.-359-51447A>G
NR_038321.1:n.85-51447A>G (OR51B5)
XM_011520010.1:c.-359-51447A>G (OR51B5)	XP_011518312.1:n.-359-51447A>G
NM_001005567.3:c.-359-51447A>G (OR51B5)	NP_001005567.2:n.-359-51447A>G
NR_038321.2:n.85-51447A>G (OR51B5)