Canonical Allele Identifier: CA2244625612

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933564A= , CM000679.2:g.4933564A= GRCh38
NC_000017.10:g.4836859A= , CM000679.1:g.4836859A= GRCh37
NC_000017.9:g.4777639A= NCBI36
NG_008767.2:g.6270A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.960A= (GP1BA) MANE Select ENSP00000329380.5:p.Thr320=
ENST00000649830.1:c.-888+778T= (CHRNE) ENSP00000496907.1:n.-888+778T=
ENST00000329125.5:c.960A= (GP1BA) ENSP00000329380.5:p.Thr320=
ENST00000611961.1:c.960A= (GP1BA) ENSP00000484439.1:p.Thr320=
NM_000173.6:c.960A= (GP1BA) NP_000164.5:p.Thr320=
NM_000173.7:c.960A= (GP1BA) MANE Select NP_000164.5:p.Thr320=