Canonical Allele Identifier: CA1949691919

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5448290A= , CM000673.2:g.5448290A= GRCh38
NC_000011.9:g.5469520A= , CM000673.1:g.5469520A= GRCh37
NC_000011.8:g.5426096A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000292896.3:c.-267+57279T= (HBE1) ENSP00000292896.2:n.-267+57279T=
ENST00000380252.6:c.-74+57061T= (HBG2) ENSP00000369602.2:n.-74+57061T=
ENST00000380259.7:c.983-102391T= ENSP00000369609.3:n.983-102391T=
ENST00000415970.6:n.84+57279T= (OR51B5)
ENST00000418729.1:n.84+57279T= (OR51B5)
ENST00000420465.6:n.45+57279T= (OR51B5)
ENST00000420726.6:n.45+57279T= (OR51B5)
ENST00000380237.5:c.-310+57279T= (HBE1) ENSP00000369586.1:n.-310+57279T=
ENST00000380252.5:c.62+57061T= (HBG2) ENSP00000369602.1:n.62+57061T=
ENST00000380259.6:c.-564-102391T= (HBG2) ENSP00000369609.2:n.-564-102391T=
ENST00000396895.1:c.-267+57279T= (HBE1) ENSP00000380104.1:n.-267+57279T=
NM_001005567.2:c.-360+57279T= (OR51B5) NP_001005567.2:n.-360+57279T=
NR_038321.1:n.84+57279T= (OR51B5)
XM_011520010.1:c.-360+2704T= (OR51B5) XP_011518312.1:n.-360+2704T=
NM_001005567.3:c.-360+57279T= (OR51B5) NP_001005567.2:n.-360+57279T=
NR_038321.2:n.84+57279T= (OR51B5)