Canonical Allele Identifier: CA397319088

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933482A>G , CM000679.2:g.4933482A>G GRCh38
NC_000017.10:g.4836777A>G , CM000679.1:g.4836777A>G GRCh37
NC_000017.9:g.4777557A>G NCBI36
NG_008767.2:g.6188A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.878A>G (GP1BA) MANE Select ENSP00000329380.5:p.Asp293Gly
ENST00000649830.1:c.-888+860T>C (CHRNE) ENSP00000496907.1:n.-888+860T>C
ENST00000329125.5:c.878A>G (GP1BA) ENSP00000329380.5:p.Asp293Gly
ENST00000611961.1:c.878A>G (GP1BA) ENSP00000484439.1:p.Asp293Gly
NM_000173.6:c.878A>G (GP1BA) NP_000164.5:p.Asp293Gly
NM_000173.7:c.878A>G (GP1BA) MANE Select NP_000164.5:p.Asp293Gly