Canonical Allele Identifier: CA2244625318

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932825C= , CM000679.2:g.4932825C= GRCh38
NC_000017.10:g.4836120C= , CM000679.1:g.4836120C= GRCh37
NC_000017.9:g.4776900C= NCBI36
NG_008767.2:g.5531C=

Transcript Alleles

HGVS Amino-acid change
ENST00000329125.6:c.221C= (GP1BA) MANE Select ENSP00000329380.5:p.Thr74=
ENST00000649830.1:c.-888+1517G= (CHRNE) ENSP00000496907.1:n.-888+1517G=
ENST00000329125.5:c.221C= (GP1BA) ENSP00000329380.5:p.Thr74=
ENST00000611961.1:c.221C= (GP1BA) ENSP00000484439.1:p.Thr74=
NM_000173.6:c.221C= (GP1BA) NP_000164.5:p.Thr74=
NM_000173.7:c.221C= (GP1BA) MANE Select NP_000164.5:p.Thr74=